| 401917705 | CV2827792 | single nucleotide variant | NM_197941.4(ADAMTS6):c.844-4T>G | not provided [RCV003429656] | uncertain significance | 5 | 65452220 | 65452220 | Human | | name |
| 8581165 | CV115602 | single nucleotide variant | NM_197941.2(ADAMTS6):c.1512+3278A>G | Lung cancer [RCV000096125] | uncertain significance | 5 | 65288051 | 65288051 | Human | | name |
| 329355565 | CV2445491 | single nucleotide variant | NM_197941.4(ADAMTS6):c.36G>C (p.Leu12Phe) | not specified [RCV004257549] | uncertain significance | 5 | 65473638 | 65473638 | Human | | name |
| 405676881 | CV3239269 | single nucleotide variant | NM_197941.4(ADAMTS6):c.78G>T (p.Arg26Ser) | not specified [RCV004370151] | uncertain significance | 5 | 65473596 | 65473596 | Human | | name |
| 329392640 | CV2471445 | single nucleotide variant | NM_197941.4(ADAMTS6):c.227T>G (p.Ile76Ser) | not specified [RCV004280443] | uncertain significance | 5 | 65471013 | 65471013 | Human | | name |
| 401734738 | CV2688604 | single nucleotide variant | NM_197941.4(ADAMTS6):c.244G>A (p.Val82Ile) | not specified [RCV004301559] | uncertain significance | 5 | 65470996 | 65470996 | Human | | name |
| 405295032 | CV3210919 | single nucleotide variant | NM_197941.4(ADAMTS6):c.269C>T (p.Ser90Leu) | ADAMTS6-related disorder [RCV003936934] | likely benign | 5 | 65470971 | 65470971 | Human | 1 | name , trait , alternate_id |
| 407462587 | CV3419452 | single nucleotide variant | NM_197941.4(ADAMTS6):c.197A>G (p.His66Arg) | not specified [RCV004612987] | uncertain significance | 5 | 65471043 | 65471043 | Human | | name |
| 598194061 | CV3940519 | single nucleotide variant | NM_197941.4(ADAMTS6):c.215G>A (p.Ser72Asn) | not specified [RCV005313098] | uncertain significance | 5 | 65471025 | 65471025 | Human | | name |
| 156234406 | CV2271136 | single nucleotide variant | NM_197941.4(ADAMTS6):c.608A>T (p.Asp203Val) | not specified [RCV004134512] | uncertain significance | 5 | 65460193 | 65460193 | Human | | name |
| 156003118 | CV2288231 | single nucleotide variant | NM_197941.4(ADAMTS6):c.731G>A (p.Arg244Lys) | not specified [RCV004149742] | uncertain significance | 5 | 65452819 | 65452819 | Human | | name |
| 329353680 | CV2467054 | single nucleotide variant | NM_197941.4(ADAMTS6):c.437T>C (p.Val146Ala) | not specified [RCV004282794] | uncertain significance | 5 | 65470803 | 65470803 | Human | | name |
| 405277040 | CV3192635 | single nucleotide variant | NM_197941.4(ADAMTS6):c.464A>G (p.His155Arg) | ADAMTS6-related disorder [RCV003917314] | likely benign | 5 | 65460337 | 65460337 | Human | | name , trait , alternate_id |
| 405294684 | CV3215573 | single nucleotide variant | NM_197941.4(ADAMTS6):c.653C>T (p.Pro218Leu) | ADAMTS6-related disorder [RCV003934604] | likely benign | 5 | 65452897 | 65452897 | Human | | name , trait , alternate_id |
| 405676161 | CV3239235 | single nucleotide variant | NM_197941.4(ADAMTS6):c.371A>C (p.Lys124Thr) | not specified [RCV004370117] | uncertain significance | 5 | 65470869 | 65470869 | Human | | name |
| 405676259 | CV3239255 | single nucleotide variant | NM_197941.4(ADAMTS6):c.700A>G (p.Asn234Asp) | not specified [RCV004370137] | uncertain significance | 5 | 65452850 | 65452850 | Human | | name |
| 407462527 | CV3419434 | single nucleotide variant | NM_197941.4(ADAMTS6):c.605A>G (p.Tyr202Cys) | not specified [RCV004612969] | uncertain significance | 5 | 65460196 | 65460196 | Human | | name |
| 408378479 | CV3500942 | single nucleotide variant | NM_197941.4(ADAMTS6):c.629C>T (p.Ser210Leu) | not provided [RCV004722592] | uncertain significance | 5 | 65460172 | 65460172 | Human | | name |
| 597797077 | CV3659687 | single nucleotide variant | NM_197941.4(ADAMTS6):c.859C>T (p.Arg287Cys) | not specified [RCV004904234] | uncertain significance | 5 | 65452201 | 65452201 | Human | | name |
| 597797127 | CV3659705 | single nucleotide variant | NM_197941.4(ADAMTS6):c.743T>C (p.Ile248Thr) | not specified [RCV004904251] | likely benign | 5 | 65452807 | 65452807 | Human | | name |
| 597797194 | CV3659733 | single nucleotide variant | NM_197941.4(ADAMTS6):c.433A>G (p.Lys145Glu) | not specified [RCV004904272] | uncertain significance | 5 | 65470807 | 65470807 | Human | | name |
| 597797197 | CV3659739 | single nucleotide variant | NM_197941.4(ADAMTS6):c.668A>G (p.Asp223Gly) | not specified [RCV004904273] | uncertain significance | 5 | 65452882 | 65452882 | Human | | name |
| 597797263 | CV3659763 | single nucleotide variant | NM_197941.4(ADAMTS6):c.407A>G (p.Tyr136Cys) | not specified [RCV004904294] | uncertain significance | 5 | 65470833 | 65470833 | Human | | name |
| 597797292 | CV3659786 | single nucleotide variant | NM_197941.4(ADAMTS6):c.563A>C (p.His188Pro) | not specified [RCV004904303] | uncertain significance | 5 | 65460238 | 65460238 | Human | | name |
| 598194051 | CV3940516 | single nucleotide variant | NM_197941.4(ADAMTS6):c.596G>A (p.Arg199Gln) | not specified [RCV005313096] | uncertain significance | 5 | 65460205 | 65460205 | Human | | name |
| 8631675 | CV86879 | single nucleotide variant | NM_197941.2(ADAMTS6):c.455T>G (p.Val152Gly) | Malignant melanoma [RCV000066970] | not provided | 5 | 65470785 | 65470785 | Human | | name |
| 156314958 | CV2196721 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2091G>T (p.Leu697Phe) | not specified [RCV004069405] | uncertain significance | 5 | 65225024 | 65225024 | Human | | name |
| 155963483 | CV2197923 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2302A>G (p.Ile768Val) | not specified [RCV004077142] | uncertain significance | 5 | 65215458 | 65215458 | Human | | name |
| 156283282 | CV2249744 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1163G>A (p.Ser388Asn) | not specified [RCV004122514] | uncertain significance | 5 | 65329438 | 65329438 | Human | | name |
| 156029989 | CV2278677 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1745T>G (p.Leu582Arg) | not specified [RCV004134875] | uncertain significance | 5 | 65262838 | 65262838 | Human | | name |
| 156276901 | CV2287781 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1348G>T (p.Asp450Tyr) | not specified [RCV004143230] | uncertain significance | 5 | 65300007 | 65300007 | Human | | name |
| 156271086 | CV2290259 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1847C>T (p.Ser616Phe) | not specified [RCV004152908] | uncertain significance | 5 | 65242190 | 65242190 | Human | | name |
| 156297926 | CV2310568 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1319A>G (p.Asn440Ser) | not specified [RCV004163585] | uncertain significance | 5 | 65300036 | 65300036 | Human | | name |
| 156194365 | CV2322111 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1274A>G (p.His425Arg) | not specified [RCV004173852] | uncertain significance | 5 | 65300081 | 65300081 | Human | | name |
| 155985751 | CV2344549 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1619G>A (p.Gly540Glu) | not specified [RCV004197329] | uncertain significance | 5 | 65273341 | 65273341 | Human | | name |
| 156122995 | CV2349984 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1861G>C (p.Glu621Gln) | not specified [RCV004199912] | uncertain significance | 5 | 65242176 | 65242176 | Human | | name |
| 156087880 | CV2366430 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2727G>C (p.Leu909Phe) | not specified [RCV004212474] | uncertain significance | 5 | 65188199 | 65188199 | Human | | name |
| 155998010 | CV2393375 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2791G>A (p.Gly931Arg) | not specified [RCV004228877] | uncertain significance | 5 | 65188135 | 65188135 | Human | | name |
| 329358495 | CV2425273 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1775G>C (p.Gly592Ala) | not specified [RCV004250943] | uncertain significance | 5 | 65260655 | 65260655 | Human | | name |
| 401770339 | CV2711090 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1940T>G (p.Val647Gly) | not specified [RCV004310777] | uncertain significance | 5 | 65226213 | 65226213 | Human | | name |
| 401742537 | CV2715254 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2977A>G (p.Lys993Glu) | not specified [RCV004324599] | uncertain significance | 5 | 65172942 | 65172942 | Human | | name |
| 401783941 | CV2720881 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1850G>A (p.Arg617Gln) | not specified [RCV004328240] | uncertain significance | 5 | 65242187 | 65242187 | Human | | name |
| 401781852 | CV2722305 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1349A>G (p.Asp450Gly) | not specified [RCV004322726] | uncertain significance | 5 | 65300006 | 65300006 | Human | | name |
| 401897405 | CV2786985 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2105G>A (p.Arg702Lys) | not specified [RCV004366113] | uncertain significance | 5 | 65225010 | 65225010 | Human | | name |
| 405675509 | CV3239105 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1147C>T (p.Pro383Ser) | not specified [RCV004369987] | uncertain significance | 5 | 65329454 | 65329454 | Human | | name |
| 405675617 | CV3239126 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1396A>G (p.Asn466Asp) | not specified [RCV004370008] | uncertain significance | 5 | 65291445 | 65291445 | Human | | name |
| 405675633 | CV3239129 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1432G>A (p.Val478Met) | not specified [RCV004370011] | uncertain significance | 5 | 65291409 | 65291409 | Human | | name |
| 405675667 | CV3239135 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1723G>C (p.Gly575Arg) | not specified [RCV004370017] | uncertain significance | 5 | 65262860 | 65262860 | Human | | name |
| 405675740 | CV3239149 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2015G>C (p.Gly672Ala) | not specified [RCV004370031] | uncertain significance | 5 | 65226138 | 65226138 | Human | | name |
| 405675966 | CV3239169 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2961G>C (p.Lys987Asn) | not specified [RCV004370051] | uncertain significance | 5 | 65172958 | 65172958 | Human | | name |
| 407462620 | CV3419462 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1744C>A (p.Leu582Ile) | not specified [RCV004612997] | uncertain significance | 5 | 65262839 | 65262839 | Human | | name |
| 407462651 | CV3419473 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1546A>G (p.Ser516Gly) | not specified [RCV004613008] | uncertain significance | 5 | 65273414 | 65273414 | Human | | name |
| 407462681 | CV3419483 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2761A>G (p.Thr921Ala) | not specified [RCV004613018] | uncertain significance | 5 | 65188165 | 65188165 | Human | | name |
| 407462714 | CV3419494 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2459T>C (p.Leu820Ser) | not specified [RCV004613029] | uncertain significance | 5 | 65214910 | 65214910 | Human | | name |
| 407462745 | CV3419505 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1786T>C (p.Tyr596His) | not specified [RCV004613040] | uncertain significance | 5 | 65260644 | 65260644 | Human | | name |
| 597797045 | CV3659676 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2032G>C (p.Asp678His) | not specified [RCV004904223] | uncertain significance | 5 | 65226121 | 65226121 | Human | | name |
| 597797171 | CV3659719 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1376G>C (p.Gly459Ala) | not specified [RCV004904265] | uncertain significance | 5 | 65291465 | 65291465 | Human | | name |
| 597797175 | CV3659725 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2183C>G (p.Pro728Arg) | not specified [RCV004904266] | uncertain significance | 5 | 65224932 | 65224932 | Human | | name |
| 597797219 | CV3659749 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2296T>A (p.Tyr766Asn) | not specified [RCV004904280] | uncertain significance | 5 | 65215464 | 65215464 | Human | | name |
| 597797241 | CV3659756 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2471A>G (p.Tyr824Cys) | not specified [RCV004904287] | uncertain significance | 5 | 65214898 | 65214898 | Human | | name |
| 597797266 | CV3659770 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1760G>A (p.Ser587Asn) | not specified [RCV004904295] | uncertain significance | 5 | 65262823 | 65262823 | Human | | name |
| 597797282 | CV3659780 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1487C>T (p.Ala496Val) | not specified [RCV004904300] | uncertain significance | 5 | 65291354 | 65291354 | Human | | name |
| 597797289 | CV3659785 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2627T>C (p.Val876Ala) | not specified [RCV004904302] | uncertain significance | 5 | 65197100 | 65197100 | Human | | name |
| 597797295 | CV3659787 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1026T>G (p.Ile342Met) | not specified [RCV004904304] | uncertain significance | 5 | 65451522 | 65451522 | Human | | name |
| 597797297 | CV3659788 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1898G>A (p.Arg633Gln) | not specified [RCV004904305] | uncertain significance | 5 | 65242139 | 65242139 | Human | | name |
| 597797300 | CV3659789 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1697T>C (p.Leu566Pro) | not specified [RCV004904306] | uncertain significance | 5 | 65262886 | 65262886 | Human | | name |
| 597797303 | CV3659790 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2032G>A (p.Asp678Asn) | not specified [RCV004904307] | uncertain significance | 5 | 65226121 | 65226121 | Human | | name |
| 597797306 | CV3659791 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1438C>G (p.Pro480Ala) | not specified [RCV004904308] | uncertain significance | 5 | 65291403 | 65291403 | Human | | name |
| 598193856 | CV3940479 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1346G>A (p.Arg449Gln) | not specified [RCV005313063] | uncertain significance | 5 | 65300009 | 65300009 | Human | | name |
| 598240854 | CV3940508 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2945G>A (p.Arg982Gln) | not specified [RCV005321452] | uncertain significance | 5 | 65172974 | 65172974 | Human | | name |
| 598194038 | CV3940514 | single nucleotide variant | NM_197941.4(ADAMTS6):c.1394A>G (p.Asp465Gly) | not specified [RCV005313094] | uncertain significance | 5 | 65291447 | 65291447 | Human | | name |
| 598240860 | CV3940518 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2230C>A (p.His744Asn) | not specified [RCV005321453] | uncertain significance | 5 | 65224362 | 65224362 | Human | | name |
| 598194068 | CV3940520 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2762C>G (p.Thr921Arg) | not specified [RCV005313099] | uncertain significance | 5 | 65188164 | 65188164 | Human | | name |
| 15151026 | CV709967 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2254A>G (p.Met752Val) | not provided [RCV000968055] | benign | 5 | 65224338 | 65224338 | Human | | name |
| 40903961 | CV918066 | single nucleotide variant | NM_197941.4(ADAMTS6):c.2840G>A (p.Arg947Gln) | Premature ovarian failure [RCV001270200] | likely pathogenic | 5 | 65188086 | 65188086 | Human | 2 | name |
| 155998067 | CV2287105 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3182G>A (p.Arg1061Gln) | not specified [RCV004144976] | uncertain significance | 5 | 65170679 | 65170679 | Human | | name |
| 156325328 | CV2335237 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3025C>G (p.Arg1009Gly) | not specified [RCV004186807] | uncertain significance | 5 | 65172894 | 65172894 | Human | | name |
| 156155477 | CV2359732 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3032G>A (p.Arg1011His) | not specified [RCV004210549] | uncertain significance | 5 | 65172887 | 65172887 | Human | | name |
| 329389756 | CV2445362 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3031C>T (p.Arg1011Cys) | not specified [RCV004263977] | uncertain significance | 5 | 65172888 | 65172888 | Human | | name |
| 401890977 | CV2778572 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3148G>C (p.Gly1050Arg) | not specified [RCV004344223] | uncertain significance | 5 | 65170713 | 65170713 | Human | | name |
| 405283571 | CV3202717 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3071C>T (p.Thr1024Ile) | ADAMTS6-related disorder [RCV003921823] | likely benign | 5 | 65172848 | 65172848 | Human | | name , trait , alternate_id |
| 405676068 | CV3239218 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3229A>G (p.Ile1077Val) | not specified [RCV004370100] | uncertain significance | 5 | 65170632 | 65170632 | Human | | name |
| 597797147 | CV3659711 | single nucleotide variant | NM_197941.4(ADAMTS6):c.3146C>T (p.Thr1049Ile) | not specified [RCV004904257] | uncertain significance | 5 | 65170715 | 65170715 | Human | | name |
