| 38463467 | CV961210 | single nucleotide variant | NM_007365.3(PADI2):c.*258A>T | Rheumatoid arthritis [RCV001249175] | association | 1 | 17068786 | 17068786 | Human | 2 | name |
| 38463471 | CV961211 | single nucleotide variant | NM_007365.3(PADI2):c.1159-39G>A | Rheumatoid arthritis [RCV001249176] | association | 1 | 17079454 | 17079454 | Human | 2 | name |
| 38463478 | CV961213 | single nucleotide variant | NM_007365.3(PADI2):c.92+1006C>A | Rheumatoid arthritis [RCV001249178] | association | 1 | 17118274 | 17118274 | Human | 2 | name |
| 156093660 | CV2252880 | single nucleotide variant | NM_007365.3(PADI2):c.7C>A (p.Arg3Ser) | not specified [RCV004120713] | uncertain significance | 1 | 17119365 | 17119365 | Human | | name |
| 156334237 | CV2230895 | single nucleotide variant | NM_007365.3(PADI2):c.10G>A (p.Glu4Lys) | not specified [RCV004092367] | uncertain significance | 1 | 17119362 | 17119362 | Human | | name |
| 401741505 | CV2680422 | single nucleotide variant | NM_007365.3(PADI2):c.64G>T (p.Gly22Cys) | not specified [RCV004288662] | uncertain significance | 1 | 17119308 | 17119308 | Human | | name |
| 598164064 | CV3995998 | single nucleotide variant | NM_007365.3(PADI2):c.95C>T (p.Ala32Val) | not specified [RCV005391095] | uncertain significance | 1 | 17105059 | 17105059 | Human | | name |
| 15201953 | CV696264 | single nucleotide variant | NM_007365.3(PADI2):c.723C>T (p.Tyr241=) | not provided [RCV000957778] | benign | 1 | 17086632 | 17086632 | Human | | name |
| 15165386 | CV706872 | single nucleotide variant | NM_007365.3(PADI2):c.342A>G (p.Thr114=) | not provided [RCV000970937] | benign | 1 | 17102994 | 17102994 | Human | | name |
| 38463474 | CV961212 | single nucleotide variant | NM_007365.3(PADI2):c.729T>G (p.Gly243=) | Rheumatoid arthritis [RCV001249177] | association | 1 | 17086626 | 17086626 | Human | 2 | name |
| 156198261 | CV2334514 | single nucleotide variant | NM_007365.3(PADI2):c.142G>A (p.Val48Met) | not specified [RCV004188476] | uncertain significance | 1 | 17105012 | 17105012 | Human | | name |
| 156121488 | CV2354255 | single nucleotide variant | NM_007365.3(PADI2):c.153G>C (p.Glu51Asp) | not specified [RCV004206677] | uncertain significance | 1 | 17105001 | 17105001 | Human | | name |
| 155905652 | CV2393120 | single nucleotide variant | NM_007365.3(PADI2):c.134C>T (p.Ser45Leu) | not specified [RCV004226600] | uncertain significance | 1 | 17105020 | 17105020 | Human | | name |
| 329373461 | CV2434259 | single nucleotide variant | NM_007365.3(PADI2):c.106G>C (p.Gly36Arg) | not specified [RCV004251934] | uncertain significance | 1 | 17105048 | 17105048 | Human | | name |
| 329353833 | CV2439758 | single nucleotide variant | NM_007365.3(PADI2):c.116C>A (p.Thr39Asn) | not specified [RCV004255764] | uncertain significance | 1 | 17105038 | 17105038 | Human | | name |
| 407517513 | CV3470070 | single nucleotide variant | NM_007365.3(PADI2):c.202C>T (p.Arg68Cys) | not specified [RCV004650682] | uncertain significance | 1 | 17104952 | 17104952 | Human | | name |
| 597694344 | CV3578349 | single nucleotide variant | NM_007365.3(PADI2):c.160C>T (p.Arg54Cys) | not specified [RCV004839018] | uncertain significance | 1 | 17104994 | 17104994 | Human | | name |
| 598164097 | CV3996003 | single nucleotide variant | NM_007365.3(PADI2):c.178G>C (p.Glu60Gln) | not specified [RCV005391100] | uncertain significance | 1 | 17104976 | 17104976 | Human | | name |
| 15185922 | CV696263 | single nucleotide variant | NM_007365.3(PADI2):c.1413C>T (p.His471=) | not provided [RCV000953128] | benign | 1 | 17075721 | 17075721 | Human | | name |
| 15132596 | CV706870 | single nucleotide variant | NM_007365.3(PADI2):c.1881C>T (p.Leu627=) | not provided [RCV000964802] | benign | 1 | 17069161 | 17069161 | Human | | name |
| 15165949 | CV731869 | single nucleotide variant | NM_007365.3(PADI2):c.1872C>T (p.Pro624=) | not provided [RCV000904335] | benign | 1 | 17069170 | 17069170 | Human | | name |
| 156148461 | CV2265277 | single nucleotide variant | NM_007365.3(PADI2):c.853A>G (p.Ile285Val) | not specified [RCV004126380] | uncertain significance | 1 | 17084684 | 17084684 | Human | | name |
| 155916098 | CV2281913 | single nucleotide variant | NM_007365.3(PADI2):c.445G>A (p.Ala149Thr) | not specified [RCV004138690] | uncertain significance | 1 | 17093651 | 17093651 | Human | | name |
| 156238435 | CV2285887 | single nucleotide variant | NM_007365.3(PADI2):c.522C>G (p.Ser174Arg) | not specified [RCV004143819] | uncertain significance | 1 | 17093574 | 17093574 | Human | | name |
| 329369608 | CV2461166 | single nucleotide variant | NM_007365.3(PADI2):c.940A>T (p.Met314Leu) | not specified [RCV004267368] | uncertain significance | 1 | 17083836 | 17083836 | Human | | name |
| 401779782 | CV2676685 | single nucleotide variant | NM_007365.3(PADI2):c.878G>A (p.Arg293Gln) | not specified [RCV004290865] | uncertain significance | 1 | 17084659 | 17084659 | Human | | name |
| 401726276 | CV2695630 | single nucleotide variant | NM_007365.3(PADI2):c.761G>A (p.Gly254Asp) | not specified [RCV004299446] | uncertain significance | 1 | 17086594 | 17086594 | Human | | name |
| 401861160 | CV2769546 | single nucleotide variant | NM_007365.3(PADI2):c.868G>A (p.Val290Met) | not specified [RCV004351199] | uncertain significance | 1 | 17084669 | 17084669 | Human | | name |
| 405741346 | CV3367539 | single nucleotide variant | NM_007365.3(PADI2):c.887C>T (p.Pro296Leu) | not specified [RCV004497789] | uncertain significance | 1 | 17084650 | 17084650 | Human | | name |
| 407517519 | CV3470073 | single nucleotide variant | NM_007365.3(PADI2):c.860C>T (p.Thr287Met) | not specified [RCV004650684] | uncertain significance | 1 | 17084677 | 17084677 | Human | | name |
| 407517522 | CV3470074 | single nucleotide variant | NM_007365.3(PADI2):c.807T>A (p.His269Gln) | not specified [RCV004650685] | uncertain significance | 1 | 17086548 | 17086548 | Human | | name |
| 407478904 | CV3470076 | single nucleotide variant | NM_007365.3(PADI2):c.468C>A (p.Asp156Glu) | not specified [RCV004664004] | uncertain significance | 1 | 17093628 | 17093628 | Human | | name |
| 597694333 | CV3578348 | single nucleotide variant | NM_007365.3(PADI2):c.782G>T (p.Gly261Val) | not specified [RCV004839017] | uncertain significance | 1 | 17086573 | 17086573 | Human | | name |
| 597657079 | CV3578351 | single nucleotide variant | NM_007365.3(PADI2):c.574G>A (p.Asp192Asn) | not specified [RCV004827576] | uncertain significance | 1 | 17092489 | 17092489 | Human | | name |
| 597657086 | CV3578353 | single nucleotide variant | NM_007365.3(PADI2):c.853A>T (p.Ile285Phe) | not specified [RCV004827577] | uncertain significance | 1 | 17084684 | 17084684 | Human | | name |
| 598164078 | CV3996000 | single nucleotide variant | NM_007365.3(PADI2):c.736G>A (p.Ala246Thr) | not specified [RCV005391097] | uncertain significance | 1 | 17086619 | 17086619 | Human | | name |
| 598164085 | CV3996001 | single nucleotide variant | NM_007365.3(PADI2):c.559C>T (p.Arg187Trp) | not specified [RCV005391098] | uncertain significance | 1 | 17092504 | 17092504 | Human | | name |
| 598164103 | CV3996004 | single nucleotide variant | NM_007365.3(PADI2):c.331C>T (p.Leu111Phe) | not specified [RCV005391101] | uncertain significance | 1 | 17103005 | 17103005 | Human | | name |
| 15155244 | CV696265 | single nucleotide variant | NM_007365.3(PADI2):c.698G>A (p.Arg233Gln) | not provided [RCV000946452] | likely benign | 1 | 17086657 | 17086657 | Human | | name |
| 155982115 | CV2272933 | single nucleotide variant | NM_007365.3(PADI2):c.1177G>A (p.Val393Met) | not specified [RCV004135823] | uncertain significance | 1 | 17079397 | 17079397 | Human | | name |
| 155903709 | CV2298666 | single nucleotide variant | NM_007365.3(PADI2):c.1734C>A (p.Asp578Glu) | not specified [RCV004156244] | uncertain significance | 1 | 17070118 | 17070118 | Human | | name |
| 155973190 | CV2335888 | single nucleotide variant | NM_007365.3(PADI2):c.1075G>A (p.Glu359Lys) | not specified [RCV004196107] | uncertain significance | 1 | 17082628 | 17082628 | Human | | name |
| 156112383 | CV2387908 | single nucleotide variant | NM_007365.3(PADI2):c.1603G>A (p.Glu535Lys) | not specified [RCV004236456] | uncertain significance | 1 | 17071438 | 17071438 | Human | | name |
| 156225769 | CV2390678 | single nucleotide variant | NM_007365.3(PADI2):c.1942G>A (p.Gly648Ser) | not specified [RCV004239193] | uncertain significance | 1 | 17069100 | 17069100 | Human | | name |
| 329379281 | CV2443356 | single nucleotide variant | NM_007365.3(PADI2):c.1463T>G (p.Leu488Arg) | not specified [RCV004260155] | likely benign | 1 | 17074942 | 17074942 | Human | | name |
| 401769753 | CV2689921 | single nucleotide variant | NM_007365.3(PADI2):c.1040G>A (p.Arg347His) | not specified [RCV004297811] | uncertain significance | 1 | 17083736 | 17083736 | Human | | name |
| 401743149 | CV2694066 | single nucleotide variant | NM_007365.3(PADI2):c.1730A>C (p.Glu577Ala) | not specified [RCV004302501] | uncertain significance | 1 | 17070122 | 17070122 | Human | | name |
| 401735489 | CV2699281 | single nucleotide variant | NM_007365.3(PADI2):c.1792C>G (p.Leu598Val) | not specified [RCV004305545] | uncertain significance | 1 | 17069250 | 17069250 | Human | | name |
| 401729988 | CV2700350 | single nucleotide variant | NM_007365.3(PADI2):c.1542G>T (p.Met514Ile) | not specified [RCV004311007] | uncertain significance | 1 | 17074863 | 17074863 | Human | | name |
| 401752593 | CV2707061 | single nucleotide variant | NM_007365.3(PADI2):c.1579A>T (p.Thr527Ser) | not specified [RCV004321647] | uncertain significance | 1 | 17071462 | 17071462 | Human | | name |
| 401721969 | CV2710260 | single nucleotide variant | NM_007365.3(PADI2):c.1171G>A (p.Gly391Ser) | not specified [RCV004317154] | uncertain significance | 1 | 17079403 | 17079403 | Human | | name |
| 401861806 | CV2756714 | single nucleotide variant | NM_007365.3(PADI2):c.1655G>A (p.Arg552His) | not specified [RCV004345221] | uncertain significance | 1 | 17070197 | 17070197 | Human | | name |
| 401896728 | CV2788720 | single nucleotide variant | NM_007365.3(PADI2):c.1232T>C (p.Leu411Pro) | not specified [RCV004361196] | uncertain significance | 1 | 17079342 | 17079342 | Human | | name |
| 405741295 | CV3367532 | single nucleotide variant | NM_007365.3(PADI2):c.1036G>A (p.Asp346Asn) | not specified [RCV004497782] | uncertain significance | 1 | 17083740 | 17083740 | Human | | name |
| 405741303 | CV3367533 | single nucleotide variant | NM_007365.3(PADI2):c.1118G>A (p.Arg373Gln) | not specified [RCV004497783] | uncertain significance | 1 | 17082585 | 17082585 | Human | | name |
| 405741311 | CV3367534 | single nucleotide variant | NM_007365.3(PADI2):c.1223T>C (p.Phe408Ser) | not specified [RCV004497784] | uncertain significance | 1 | 17079351 | 17079351 | Human | | name |
| 405741318 | CV3367535 | single nucleotide variant | NM_007365.3(PADI2):c.1447G>A (p.Gly483Ser) | not specified [RCV004497785] | uncertain significance | 1 | 17075687 | 17075687 | Human | | name |
| 405741325 | CV3367536 | single nucleotide variant | NM_007365.3(PADI2):c.1542G>A (p.Met514Ile) | not specified [RCV004497786] | uncertain significance | 1 | 17074863 | 17074863 | Human | | name |
| 405741331 | CV3367537 | single nucleotide variant | NM_007365.3(PADI2):c.1852G>A (p.Val618Met) | not specified [RCV004497787] | uncertain significance | 1 | 17069190 | 17069190 | Human | | name |
| 405741339 | CV3367538 | single nucleotide variant | NM_007365.3(PADI2):c.1855C>T (p.Arg619Cys) | not specified [RCV004497788] | uncertain significance | 1 | 17069187 | 17069187 | Human | | name |
| 407517516 | CV3470071 | single nucleotide variant | NM_007365.3(PADI2):c.1955G>A (p.Arg652His) | not specified [RCV004650683] | uncertain significance | 1 | 17069087 | 17069087 | Human | | name |
| 407478892 | CV3470072 | single nucleotide variant | NM_007365.3(PADI2):c.1729G>A (p.Glu577Lys) | not specified [RCV004664002] | likely benign | 1 | 17070123 | 17070123 | Human | | name |
| 407478898 | CV3470075 | single nucleotide variant | NM_007365.3(PADI2):c.1321C>T (p.Arg441Trp) | not specified [RCV004664003] | uncertain significance | 1 | 17075813 | 17075813 | Human | | name |
| 407517525 | CV3470077 | single nucleotide variant | NM_007365.3(PADI2):c.1286T>C (p.Ile429Thr) | not specified [RCV004650686] | uncertain significance | 1 | 17079288 | 17079288 | Human | | name |
| 407478909 | CV3470078 | single nucleotide variant | NM_007365.3(PADI2):c.1039C>T (p.Arg347Cys) | not specified [RCV004664005] | uncertain significance | 1 | 17083737 | 17083737 | Human | | name |
| 597694354 | CV3578350 | single nucleotide variant | NM_007365.3(PADI2):c.1274C>T (p.Pro425Leu) | not specified [RCV004839019] | uncertain significance | 1 | 17079300 | 17079300 | Human | | name |
| 597694365 | CV3578352 | single nucleotide variant | NM_007365.3(PADI2):c.1192C>T (p.Leu398Phe) | not specified [RCV004839020] | uncertain significance | 1 | 17079382 | 17079382 | Human | | name |
| 597694374 | CV3578355 | single nucleotide variant | NM_007365.3(PADI2):c.1322G>A (p.Arg441Gln) | not specified [RCV004839021] | uncertain significance | 1 | 17075812 | 17075812 | Human | | name |
| 597694625 | CV3578356 | single nucleotide variant | NM_007365.3(PADI2):c.1337T>C (p.Val446Ala) | not specified [RCV004839022] | uncertain significance | 1 | 17075797 | 17075797 | Human | | name |
| 598164058 | CV3995997 | single nucleotide variant | NM_007365.3(PADI2):c.1676T>C (p.Leu559Pro) | not specified [RCV005391094] | uncertain significance | 1 | 17070176 | 17070176 | Human | | name |
| 598164070 | CV3995999 | single nucleotide variant | NM_007365.3(PADI2):c.1539C>G (p.Ile513Met) | not specified [RCV005391096] | uncertain significance | 1 | 17074866 | 17074866 | Human | | name |
| 598164091 | CV3996002 | single nucleotide variant | NM_007365.3(PADI2):c.1505G>A (p.Arg502Gln) | not specified [RCV005391099] | uncertain significance | 1 | 17074900 | 17074900 | Human | | name |
| 598164113 | CV3996006 | single nucleotide variant | NM_007365.3(PADI2):c.1327A>G (p.Met443Val) | not specified [RCV005391103] | uncertain significance | 1 | 17075807 | 17075807 | Human | | name |
| 15130489 | CV706871 | single nucleotide variant | NM_007365.3(PADI2):c.1018C>T (p.Gln340Ter) | not provided [RCV000964444] | likely benign | 1 | 17083758 | 17083758 | Human | | name |
