ClinVar Miner

List of variants in gene ABCC9 studied for Familial atrial fibrillation

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Total variants: 36
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HGVS dbSNP
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.1165-6del rs35857705
NM_005691.3(ABCC9):c.1165-7_1165-6del rs35857705
NM_005691.3(ABCC9):c.1296= (p.Pro432=) rs10770865
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.1557G>A (p.Glu519=) rs143346402
NM_005691.3(ABCC9):c.1659+10T>C rs201753781
NM_005691.3(ABCC9):c.1670C>G (p.Thr557Ser) rs886049171
NM_005691.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
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.2238-17del rs4148670
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
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.2862C>T (p.Asp954=) rs2291550
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.372T>C (p.Asn124=) rs377384557
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.574-5C>A rs3759236
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.1164+11A>G rs4762720
NM_020297.3(ABCC9):c.2199-11T>C rs697250

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