ClinVar Miner

List of variants in gene ABCC9 studied for atrial fibrillation, familial, 12

Included ClinVar conditions (4):
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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_020297.4(ABCC9):c.1848C>T (p.Asp616=) rs61001398 0.01493
NM_020297.4(ABCC9):c.3315+17C>T rs200692327 0.00023
NM_020297.4(ABCC9):c.3669G>A (p.Thr1223=) rs146942382 0.00016
NM_020297.4(ABCC9):c.4512+765C>T rs142875103 0.00016
NM_020297.4(ABCC9):c.1987C>T (p.Arg663Cys) rs200349671 0.00014
NM_020297.4(ABCC9):c.2339+13A>G rs189255166 0.00012
NM_020297.4(ABCC9):c.142+10C>A rs138917284 0.00007
NM_020297.4(ABCC9):c.1979G>A (p.Arg660Gln) rs150255709 0.00006
NM_020297.4(ABCC9):c.4512+711G>A rs72559751 0.00006
NM_020297.4(ABCC9):c.4512+777G>A rs542730918 0.00005
NM_020297.4(ABCC9):c.1849G>A (p.Asp617Asn) rs757681761 0.00004
NM_020297.4(ABCC9):c.2599G>A (p.Val867Ile) rs376754153 0.00004
NM_020297.4(ABCC9):c.3061G>A (p.Glu1021Lys) rs749668601 0.00004
NM_020297.4(ABCC9):c.4205C>G (p.Ser1402Cys) rs369587958 0.00004
NM_020297.4(ABCC9):c.1012-7G>A rs727502874 0.00003
NM_020297.4(ABCC9):c.1329G>A (p.Met443Ile) rs151197166 0.00003
NM_020297.4(ABCC9):c.2312C>T (p.Thr771Ile) rs180739851 0.00003
NM_020297.4(ABCC9):c.2857G>A (p.Glu953Lys) rs143685061 0.00003
NM_020297.4(ABCC9):c.3594G>A (p.Met1198Ile) rs199900459 0.00003
NM_020297.4(ABCC9):c.4535C>T (p.Thr1512Met) rs554811993 0.00003
NM_020297.4(ABCC9):c.1828_1829del (p.Leu610fs) rs776934642 0.00002
NM_020297.4(ABCC9):c.3462G>A (p.Arg1154=) rs1336342134 0.00002
NM_020297.4(ABCC9):c.3590G>A (p.Arg1197His) rs755156050 0.00002
NM_020297.4(ABCC9):c.575G>A (p.Arg192Lys) rs727504612 0.00002
NM_020297.4(ABCC9):c.1012-2A>G rs1345994016 0.00001
NM_020297.4(ABCC9):c.1129A>G (p.Ile377Val) rs567016348 0.00001
NM_020297.4(ABCC9):c.1147C>T (p.Leu383Phe) rs755542764 0.00001
NM_020297.4(ABCC9):c.1603T>C (p.Tyr535His) rs397517184 0.00001
NM_020297.4(ABCC9):c.1671C>A (p.Thr557=) rs746467455 0.00001
NM_020297.4(ABCC9):c.1743G>A (p.Leu581=) rs777049470 0.00001
NM_020297.4(ABCC9):c.1978C>T (p.Arg660Trp) rs760889253 0.00001
NM_020297.4(ABCC9):c.2215C>G (p.Pro739Ala) rs201223488 0.00001
NM_020297.4(ABCC9):c.2865A>T (p.Glu955Asp) rs922212635 0.00001
NM_020297.4(ABCC9):c.3283C>T (p.Arg1095Cys) rs752450127 0.00001
NM_020297.4(ABCC9):c.395A>G (p.Lys132Arg) rs727505161 0.00001
NM_020297.4(ABCC9):c.4189A>G (p.Ile1397Val) rs1162169303 0.00001
NM_020297.4(ABCC9):c.5G>A (p.Ser2Asn) rs1359649036 0.00001
NM_020297.4(ABCC9):c.1657G>T (p.Ala553Ser) rs2137747839
NM_020297.4(ABCC9):c.1975A>G (p.Thr659Ala) rs878854783
NM_020297.4(ABCC9):c.2080C>T (p.Arg694Ter) rs1194330942
NM_020297.4(ABCC9):c.2470C>T (p.Arg824Ter) rs779866340
NM_020297.4(ABCC9):c.2818G>T (p.Ala940Ser) rs1373377020
NM_020297.4(ABCC9):c.2928_2929dup (p.Met977fs) rs1565731854
NM_020297.4(ABCC9):c.295T>A (p.Ser99Thr) rs1270249014
NM_020297.4(ABCC9):c.3492_3493del (p.Asp1164fs)
NM_020297.4(ABCC9):c.4014del (p.Gly1339fs) rs2137173765
NM_020297.4(ABCC9):c.4196dup (p.Ser1400fs) rs730880370
NM_020297.4(ABCC9):c.4450-6_4450-5del rs4148680
NM_020297.4(ABCC9):c.4512+746_4512+747insT rs761784169
NM_020297.4(ABCC9):c.4512+814C>T rs387906805
NM_020297.4(ABCC9):c.4512+824G>C rs1941745235
NM_020297.4(ABCC9):c.723G>T (p.Lys241Asn) rs1948578084
NM_020297.4(ABCC9):c.7C>G (p.Leu3Val) rs976596252

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