ClinVar Miner

List of variants reported as uncertain significance for Familial atrial fibrillation by Illumina Clinical Services Laboratory,Illumina

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ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_000218.2(KCNQ1):c.29C>A (p.Ala10Asp) rs886048161
NM_000218.2(KCNQ1):c.66C>T (p.Gly22=) rs886048162
NM_000891.2(KCNJ2):c.*1128dup rs777658732
NM_000891.2(KCNJ2):c.*1702_*1704dup rs1555604193
NM_000891.2(KCNJ2):c.*1702dup rs886053334
NM_000891.2(KCNJ2):c.*1704_*1705dupCT rs1555604187
NM_000891.2(KCNJ2):c.*1719_*1721dup rs35753731
NM_000891.2(KCNJ2):c.*1720_*1721dup rs35753731
NM_000891.2(KCNJ2):c.*1721dup rs35753731
NM_000891.2(KCNJ2):c.*2770_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2771_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2772_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2774_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2775dup rs35656864
NM_000891.2(KCNJ2):c.*2776del rs886053343
NM_000891.2(KCNJ2):c.*2875_*2876del rs561353262
NM_000891.2(KCNJ2):c.*324del rs570173316
NM_000891.2(KCNJ2):c.*3391_*3392dup rs552636156
NM_000891.2(KCNJ2):c.*3463del rs3841509
NM_000891.2(KCNJ2):c.-162delinsTCAGAGTAGT rs376713253
NM_000891.2(KCNJ2):c.-88C>T rs886053322
NM_000891.2(KCNJ2):c.1259C>T (p.Pro420Leu) rs749707062
NM_005266.6(GJA5):c.-67G>A rs36214923
NM_005691.3(ABCC9):c.-11T>C rs72559432
NM_005691.3(ABCC9):c.1165-19dup rs35857705
NM_005691.3(ABCC9):c.1165-4del rs886049172
NM_005691.3(ABCC9):c.1165-7_1165-6del rs35857705
NM_005691.3(ABCC9):c.1332C>T (p.Gly444=) rs369830406
NM_005691.3(ABCC9):c.146G>C (p.Trp49Ser) rs886049175
NM_005691.3(ABCC9):c.1659+10T>C rs201753781
NM_005691.3(ABCC9):c.1670C>G (p.Thr557Ser) rs886049171
NM_005691.3(ABCC9):c.1992C>T (p.Pro664=) rs780071007
NM_005691.3(ABCC9):c.2199-6T>C rs535477725
NM_005691.3(ABCC9):c.2238-16del rs886049170
NM_005691.3(ABCC9):c.2644-11G>A rs61926078
NM_005691.3(ABCC9):c.2769+12T>C rs564071879
NM_005691.3(ABCC9):c.2770-13A>G rs184123387
NM_005691.3(ABCC9):c.2826T>C (p.Tyr942=) rs141025897
NM_005691.3(ABCC9):c.3556C>T (p.Arg1186Trp) rs886049169
NM_005691.3(ABCC9):c.3669+10T>C rs199640712
NM_005691.3(ABCC9):c.366T>C (p.Tyr122=) rs886049174
NM_005691.3(ABCC9):c.407-14C>A rs201279882
NM_005691.3(ABCC9):c.4316-14T>G rs886049168
NM_005691.3(ABCC9):c.466T>C (p.Cys156Arg) rs886049173
NM_005691.3(ABCC9):c.669G>T (p.Leu223=) rs17846788
NM_005691.3(ABCC9):c.75T>C (p.Phe25=) rs201972673
NM_005691.3(ABCC9):c.842G>A (p.Arg281Gln) rs753456211
NM_020297.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_020297.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_020297.3(ABCC9):c.372T>C (p.Asn124=) rs377384557
NM_172201.1(KCNE2):c.-121C>T rs188625398
NM_181703.4(GJA5):c.*1211A>G rs886045244
NM_181703.4(GJA5):c.*1259C>T rs886045243
NM_181798.1(KCNQ1):c.*160C>A rs886048167
NM_181798.1(KCNQ1):c.*26C>A rs886048166
NM_181798.1(KCNQ1):c.*292C>A rs886048169
NM_181798.1(KCNQ1):c.*398C>T rs886048170
NM_181798.1(KCNQ1):c.*554T>G rs886048172
NM_181798.1(KCNQ1):c.*887_*889del rs886048175
NM_181798.1(KCNQ1):c.*897G>T rs561861522
NM_181798.1(KCNQ1):c.1133+3G>A rs374767819
NM_181798.1(KCNQ1):c.1592C>A (p.Thr531Asn) rs377661455
NM_181798.1(KCNQ1):c.1598C>A (p.Pro533His) rs886048165
NM_181798.1(KCNQ1):c.269C>T (p.Ser90Phe) rs886048163
NM_181798.1(KCNQ1):c.400-6G>T rs886048164
NM_181798.1(KCNQ1):c.808C>T (p.Arg270Trp) rs199472776
NM_181798.1(KCNQ1):c.870+13C>T rs201364493
NM_181798.1(KCNQ1):c.974G>A (p.Arg325Gln) rs145229963

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