| 12838397 | CV369602 | single nucleotide variant | NM_005260.7(GDF9):c.-32A>G | not specified [RCV000426886] | benign | 5 | 132864565 | 132864565 | Human | | name |
| 150495708 | CV1283038 | single nucleotide variant | NM_005260.7(GDF9):c.-103C>A | not provided [RCV001717444] | benign | 5 | 132864636 | 132864636 | Human | | name |
| 598158523 | CV3896816 | single nucleotide variant | NM_005260.7(GDF9):c.-1088A>G | Premature ovarian failure 14 [RCV005367879] | uncertain significance | 5 | 132865621 | 132865621 | Human | 1 | name |
| 150456344 | CV1219473 | single nucleotide variant | NM_005260.7(GDF9):c.398-39G>C | not provided [RCV001612688] | benign | 5 | 132862595 | 132862595 | Human | | name |
| 14698887 | CV623766 | duplication | NM_005260.7(GDF9):c.-616_-142dup | Premature ovarian failure [RCV000787459] | uncertain significance | 5 | 132864674 | 132864675 | Human | 2 | name |
| 156175554 | CV2205255 | single nucleotide variant | NM_005260.7(GDF9):c.7C>T (p.Arg3Cys) | not specified [RCV004079882] | uncertain significance | 5 | 132864527 | 132864527 | Human | | name |
| 405258310 | CV3203179 | single nucleotide variant | NM_005260.7(GDF9):c.205C>T (p.Leu69=) | GDF9-related disorder [RCV003941787] | likely benign | 5 | 132864329 | 132864329 | Human | | name , trait , alternate_id |
| 150501531 | CV1224209 | single nucleotide variant | NM_005260.7(GDF9):c.447C>T (p.Thr149=) | GDF9-related disorder [RCV003980797]|not provided [RCV001620850] | benign | 5 | 132862507 | 132862507 | Human | 1 | name , trait , alternate_id |
| 8691202 | CV141162 | single nucleotide variant | NM_005260.7(GDF9):c.546G>A (p.Glu182=) | GDF9-related disorder [RCV003975108]|not specified [RCV000125220] | benign | 5 | 132862408 | 132862408 | Human | 1 | name , trait , alternate_id |
| 156211072 | CV2370317 | single nucleotide variant | NM_005260.7(GDF9):c.85G>A (p.Gly29Arg) | not specified [RCV004213228] | likely benign | 5 | 132864449 | 132864449 | Human | | name |
| 401917849 | CV2827996 | single nucleotide variant | NM_005260.7(GDF9):c.421C>T (p.Leu141=) | not provided [RCV003429767] | uncertain significance | 5 | 132862533 | 132862533 | Human | | name |
| 407512530 | CV3432933 | single nucleotide variant | NM_005260.7(GDF9):c.98A>G (p.Gln33Arg) | not specified [RCV004626855] | uncertain significance | 5 | 132864436 | 132864436 | Human | | name |
| 407512615 | CV3432936 | single nucleotide variant | NM_005260.7(GDF9):c.73T>G (p.Ser25Ala) | not specified [RCV004626858] | uncertain significance | 5 | 132864461 | 132864461 | Human | | name |
| 407512619 | CV3432937 | single nucleotide variant | NM_005260.7(GDF9):c.74C>T (p.Ser25Phe) | not specified [RCV004626859] | uncertain significance | 5 | 132864460 | 132864460 | Human | | name |
| 150502747 | CV1241637 | single nucleotide variant | NM_005260.7(GDF9):c.169G>T (p.Asp57Tyr) | GDF9-related disorder [RCV003910944]|not provided [RCV001657228] | benign | 5 | 132864365 | 132864365 | Human | 1 | name , trait , alternate_id |
| 156152863 | CV2209399 | single nucleotide variant | NM_005260.7(GDF9):c.176C>T (p.Ala59Val) | not specified [RCV004093564] | uncertain significance | 5 | 132864358 | 132864358 | Human | | name |
| 156170041 | CV2380550 | single nucleotide variant | NM_005260.7(GDF9):c.125C>T (p.Ser42Phe) | not specified [RCV004224873] | uncertain significance | 5 | 132864409 | 132864409 | Human | | name |
| 401916410 | CV2831073 | single nucleotide variant | NM_005260.7(GDF9):c.1353C>T (p.Cys451=) | not provided [RCV003443342] | likely benign | 5 | 132861601 | 132861601 | Human | | name |
| 405696425 | CV3226729 | single nucleotide variant | NM_005260.7(GDF9):c.1245A>C (p.Pro415=) | not provided [RCV003993122] | likely benign | 5 | 132861709 | 132861709 | Human | | name |
| 405785772 | CV3258113 | single nucleotide variant | NM_005260.7(GDF9):c.109A>G (p.Ser37Gly) | not specified [RCV004387616] | uncertain significance | 5 | 132864425 | 132864425 | Human | | name |
| 405785777 | CV3258114 | single nucleotide variant | NM_005260.7(GDF9):c.190G>A (p.Ala64Thr) | not specified [RCV004387617] | uncertain significance | 5 | 132864344 | 132864344 | Human | | name |
| 597758374 | CV3687750 | single nucleotide variant | NM_005260.7(GDF9):c.115G>A (p.Glu39Lys) | not specified [RCV004925276] | uncertain significance | 5 | 132864419 | 132864419 | Human | | name |
| 13674097 | CV536009 | deletion | NM_005260.7(GDF9):c.783del (p.Ser262fs) | Premature ovarian failure 14 [RCV000656489] | pathogenic|not provided | 5 | 132862171 | 132862171 | Human | 1 | name |
| 150512904 | CV1245936 | single nucleotide variant | NM_005260.7(GDF9):c.946C>T (p.Arg316Cys) | Genetic non-acquired premature ovarian failure [RCV001661766] | likely pathogenic | 5 | 132862008 | 132862008 | Human | 2 | name |
| 155798191 | CV1861899 | single nucleotide variant | NM_005260.7(GDF9):c.604C>T (p.Gln202Ter) | Premature ovarian failure 14 [RCV002471302] | uncertain significance | 5 | 132862350 | 132862350 | Human | 1 | name |
| 156365643 | CV2193243 | single nucleotide variant | NM_005260.7(GDF9):c.448G>A (p.Val150Ile) | not specified [RCV004071226] | uncertain significance | 5 | 132862506 | 132862506 | Human | | name |
| 156366321 | CV2203304 | single nucleotide variant | NM_005260.7(GDF9):c.356C>T (p.Pro119Leu) | not specified [RCV004071335] | uncertain significance | 5 | 132864178 | 132864178 | Human | | name |
| 156028280 | CV2238212 | single nucleotide variant | NM_005260.7(GDF9):c.377C>T (p.Ala126Val) | not specified [RCV004113304] | likely benign | 5 | 132864157 | 132864157 | Human | | name |
| 156014444 | CV2300548 | single nucleotide variant | NM_005260.7(GDF9):c.323G>A (p.Ser108Asn) | not specified [RCV004155516] | uncertain significance | 5 | 132864211 | 132864211 | Human | | name |
| 156173820 | CV2326805 | single nucleotide variant | NM_005260.7(GDF9):c.437G>A (p.Arg146His) | not specified [RCV004176640] | uncertain significance | 5 | 132862517 | 132862517 | Human | | name |
| 156174578 | CV2345950 | single nucleotide variant | NM_005260.7(GDF9):c.562A>G (p.Arg188Gly) | not specified [RCV004198986] | uncertain significance | 5 | 132862392 | 132862392 | Human | | name |
| 155930419 | CV2361143 | single nucleotide variant | NM_005260.7(GDF9):c.848A>G (p.Tyr283Cys) | not specified [RCV004216332] | uncertain significance | 5 | 132862106 | 132862106 | Human | | name |
| 329379280 | CV2456184 | single nucleotide variant | NM_005260.7(GDF9):c.479A>G (p.Tyr160Cys) | not specified [RCV004273373] | uncertain significance | 5 | 132862475 | 132862475 | Human | | name |
| 329381364 | CV2464662 | single nucleotide variant | NM_005260.7(GDF9):c.674C>T (p.Ala225Val) | not specified [RCV004278341] | uncertain significance | 5 | 132862280 | 132862280 | Human | | name |
| 329397446 | CV2466201 | single nucleotide variant | NM_005260.7(GDF9):c.511G>T (p.Ala171Ser) | not specified [RCV004279843] | uncertain significance | 5 | 132862443 | 132862443 | Human | | name |
| 401887851 | CV2772234 | single nucleotide variant | NM_005260.7(GDF9):c.874G>T (p.Asp292Tyr) | not specified [RCV004346872] | uncertain significance | 5 | 132862080 | 132862080 | Human | | name |
| 405785782 | CV3258115 | single nucleotide variant | NM_005260.7(GDF9):c.454C>T (p.His152Tyr) | not specified [RCV004387618] | uncertain significance | 5 | 132862500 | 132862500 | Human | | name |
| 405785788 | CV3258117 | single nucleotide variant | NM_005260.7(GDF9):c.749A>C (p.Gln250Pro) | not specified [RCV004387620] | uncertain significance | 5 | 132862205 | 132862205 | Human | | name |
| 407429771 | CV3414230 | single nucleotide variant | NM_005260.7(GDF9):c.794T>G (p.Leu265Ter) | Premature ovarian failure 14 [RCV004595816] | pathogenic|not provided | 5 | 132862160 | 132862160 | Human | 1 | name |
| 407512522 | CV3432931 | single nucleotide variant | NM_005260.7(GDF9):c.571G>A (p.Gly191Ser) | not specified [RCV004626853] | uncertain significance | 5 | 132862383 | 132862383 | Human | | name |
| 407512612 | CV3432935 | single nucleotide variant | NM_005260.7(GDF9):c.636T>G (p.Ile212Met) | not specified [RCV004626857] | uncertain significance | 5 | 132862318 | 132862318 | Human | | name |
| 597704334 | CV3687745 | single nucleotide variant | NM_005260.7(GDF9):c.992C>T (p.Pro331Leu) | not specified [RCV004916711] | uncertain significance | 5 | 132861962 | 132861962 | Human | | name |
| 597758368 | CV3687749 | single nucleotide variant | NM_005260.7(GDF9):c.991C>A (p.Pro331Thr) | not specified [RCV004925275] | uncertain significance | 5 | 132861963 | 132861963 | Human | | name |
| 597758379 | CV3687751 | single nucleotide variant | NM_005260.7(GDF9):c.364C>T (p.Arg122Trp) | not specified [RCV004925277] | uncertain significance | 5 | 132864170 | 132864170 | Human | | name |
| 597758384 | CV3687752 | single nucleotide variant | NM_005260.7(GDF9):c.527G>A (p.Cys176Tyr) | not specified [RCV004925278] | uncertain significance | 5 | 132862427 | 132862427 | Human | | name |
| 597704291 | CV3687753 | single nucleotide variant | NM_005260.7(GDF9):c.614T>C (p.Phe205Ser) | not specified [RCV004916715] | uncertain significance | 5 | 132862340 | 132862340 | Human | | name |
| 597758388 | CV3687754 | single nucleotide variant | NM_005260.7(GDF9):c.686G>A (p.Arg229Lys) | not specified [RCV004925279] | uncertain significance | 5 | 132862268 | 132862268 | Human | | name |
| 616940171 | CV4014680 | single nucleotide variant | NM_005260.7(GDF9):c.307C>T (p.Pro103Ser) | not provided [RCV005414174] | uncertain significance | 5 | 132864227 | 132864227 | Human | | name |
| 616940211 | CV4014720 | single nucleotide variant | NM_005260.7(GDF9):c.952C>T (p.Arg318Cys) | not provided [RCV005414214] | uncertain significance | 5 | 132862002 | 132862002 | Human | | name |
| 8625905 | CV81029 | single nucleotide variant | NM_005260.4(GDF9):c.379C>T (p.Pro127Ser) | Malignant melanoma [RCV000061107] | not provided | 5 | 132864155 | 132864155 | Human | | name |
| 150512896 | CV1245930 | single nucleotide variant | NM_005260.7(GDF9):c.1283G>C (p.Ser428Thr) | Genetic non-acquired premature ovarian failure [RCV001661760]|Premature ovarian failure 14 [RCV004796649] | likely pathogenic|uncertain significance | 5 | 132861671 | 132861671 | Human | 3 | name |
| 150520390 | CV1289574 | single nucleotide variant | NM_005260.7(GDF9):c.1364A>C (p.Ter455Ser) | Premature ovarian failure 14 [RCV001729991] | likely pathogenic | 5 | 132861590 | 132861590 | Human | 1 | name |
| 156154048 | CV2209495 | single nucleotide variant | NM_005260.7(GDF9):c.1232A>G (p.Asp411Gly) | not specified [RCV004093626] | uncertain significance | 5 | 132861722 | 132861722 | Human | | name |
| 156385433 | CV2227921 | single nucleotide variant | NM_005260.7(GDF9):c.1303G>A (p.Asp435Asn) | not specified [RCV004096179] | uncertain significance | 5 | 132861651 | 132861651 | Human | | name |
| 156244060 | CV2313034 | single nucleotide variant | NM_005260.7(GDF9):c.1066C>T (p.His356Tyr) | not specified [RCV004161315] | uncertain significance | 5 | 132861888 | 132861888 | Human | | name |
| 156087373 | CV2336954 | single nucleotide variant | NM_005260.7(GDF9):c.1124A>T (p.His375Leu) | not specified [RCV004192728] | uncertain significance | 5 | 132861830 | 132861830 | Human | | name |
| 401769628 | CV2731480 | single nucleotide variant | NM_005260.7(GDF9):c.1319A>G (p.Tyr440Cys) | not specified [RCV004330834] | uncertain significance | 5 | 132861635 | 132861635 | Human | | name |
| 401726814 | CV2736183 | single nucleotide variant | NM_005260.7(GDF9):c.1360C>T (p.Arg454Cys) | not provided [RCV003312631] | likely benign|conflicting interpretations of pathogenicity | 5 | 132861594 | 132861594 | Human | | name |
| 405270042 | CV3215372 | single nucleotide variant | NM_005260.7(GDF9):c.1250C>T (p.Pro417Leu) | GDF9-related disorder [RCV003949130] | likely benign | 5 | 132861704 | 132861704 | Human | | name , trait , alternate_id |
| 405785762 | CV3258111 | single nucleotide variant | NM_005260.7(GDF9):c.1045C>G (p.Pro349Ala) | not specified [RCV004387614] | uncertain significance | 5 | 132861909 | 132861909 | Human | | name |
| 405785767 | CV3258112 | single nucleotide variant | NM_005260.7(GDF9):c.1088G>A (p.Ser363Asn) | not specified [RCV004387615] | uncertain significance | 5 | 132861866 | 132861866 | Human | | name |
| 407429770 | CV3414229 | single nucleotide variant | NM_005260.7(GDF9):c.1121C>T (p.Pro374Leu) | Premature ovarian failure 14 [RCV004595815] | pathogenic|not provided | 5 | 132861833 | 132861833 | Human | 1 | name |
| 407512526 | CV3432932 | single nucleotide variant | NM_005260.7(GDF9):c.1333G>A (p.Asp445Asn) | not specified [RCV004626854] | uncertain significance | 5 | 132861621 | 132861621 | Human | | name |
| 407512533 | CV3432934 | single nucleotide variant | NM_005260.7(GDF9):c.1220A>C (p.Tyr407Ser) | not specified [RCV004626856] | uncertain significance | 5 | 132861734 | 132861734 | Human | | name |
| 596926444 | CV3542278 | single nucleotide variant | NM_005260.7(GDF9):c.1275C>A (p.Ser425Arg) | Premature ovarian failure 14 [RCV004796493] | uncertain significance | 5 | 132861679 | 132861679 | Human | 1 | name |
| 597704324 | CV3687746 | single nucleotide variant | NM_005260.7(GDF9):c.1330G>A (p.Glu444Lys) | not specified [RCV004916712] | uncertain significance | 5 | 132861624 | 132861624 | Human | | name |
| 597704301 | CV3687748 | single nucleotide variant | NM_005260.7(GDF9):c.1108T>A (p.Trp370Arg) | not specified [RCV004916714] | uncertain significance | 5 | 132861846 | 132861846 | Human | | name |
| 597704277 | CV3687755 | single nucleotide variant | NM_005260.7(GDF9):c.1300C>T (p.Pro434Ser) | not specified [RCV004916716] | uncertain significance | 5 | 132861654 | 132861654 | Human | | name |
| 598128555 | CV3887759 | single nucleotide variant | NM_005260.7(GDF9):c.1128G>T (p.Arg376Ser) | not provided [RCV005243933] | uncertain significance | 5 | 132861826 | 132861826 | Human | | name |
| 616940221 | CV4014731 | single nucleotide variant | NM_005260.7(GDF9):c.1205T>C (p.Val402Ala) | not provided [RCV005414225] | uncertain significance | 5 | 132861749 | 132861749 | Human | | name |
| 13833777 | CV585015 | single nucleotide variant | NM_005260.7(GDF9):c.1330G>T (p.Glu444Ter) | not provided [RCV000729130] | uncertain significance | 5 | 132861624 | 132861624 | Human | | name |
| 405690463 | CV3227398 | microsatellite | NM_005260.7(GDF9):c.759_762del (p.Phe254fs) | Premature ovarian failure 14 [RCV003991742] | likely pathogenic | 5 | 132862192 | 132862195 | Human | | name |
