ClinVar Miner

List of variants reported as uncertain significance for atrial fibrillation, familial, 14

Included ClinVar conditions (1):
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_004588.5(SCN2B):c.250C>T (p.Arg84Cys) rs760669515 0.00012
NM_004588.5(SCN2B):c.205T>C (p.Tyr69His) rs369196654 0.00009
NM_004588.5(SCN2B):c.281G>A (p.Arg94Gln) rs774866184 0.00009
NM_004588.5(SCN2B):c.640G>A (p.Ala214Thr) rs200264107 0.00008
NM_004588.5(SCN2B):c.82C>T (p.Arg28Trp) rs17121819 0.00007
NM_004588.5(SCN2B):c.140G>A (p.Arg47His) rs17121818 0.00006
NM_004588.5(SCN2B):c.478G>A (p.Val160Met) rs774317271 0.00006
NM_004588.5(SCN2B):c.5A>G (p.His2Arg) rs765743471 0.00006
NM_004588.5(SCN2B):c.629C>T (p.Pro210Leu) rs144248214 0.00006
NM_004588.5(SCN2B):c.461G>A (p.Arg154Gln) rs753389706 0.00004
NM_004588.5(SCN2B):c.118G>A (p.Val40Ile) rs200761835 0.00003
NM_004588.5(SCN2B):c.349G>A (p.Val117Met) rs754755062 0.00003
NM_004588.5(SCN2B):c.410G>A (p.Arg137His) rs878854712 0.00003
NM_004588.5(SCN2B):c.152C>T (p.Thr51Ile) rs765542447 0.00002
NM_004588.5(SCN2B):c.292C>T (p.Arg98Cys) rs771234231 0.00002
NM_004588.5(SCN2B):c.295G>A (p.Val99Met) rs772817742 0.00002
NM_004588.5(SCN2B):c.44C>T (p.Thr15Met) rs201373014 0.00002
NM_004588.5(SCN2B):c.632A>G (p.Asp211Gly) rs587777023 0.00002
NM_004588.5(SCN2B):c.83G>A (p.Arg28Gln) rs72544145 0.00002
NM_004588.5(SCN2B):c.109A>G (p.Thr37Ala) rs761979593 0.00001
NM_004588.5(SCN2B):c.236T>C (p.Met79Thr) rs1192595114 0.00001
NM_004588.5(SCN2B):c.237G>C (p.Met79Ile) rs142643516 0.00001
NM_004588.5(SCN2B):c.251G>A (p.Arg84His) rs201460753 0.00001
NM_004588.5(SCN2B):c.255G>T (p.Met85Ile) rs767512158 0.00001
NM_004588.5(SCN2B):c.343A>G (p.Arg115Gly) rs758238682 0.00001
NM_004588.5(SCN2B):c.93G>T (p.Glu31Asp) rs767173208 0.00001
NC_000011.9:g.(?_118047057)_(118047146_?)del
NM_004588.5(SCN2B):c.*5T>G
NM_004588.5(SCN2B):c.110C>T (p.Thr37Ile)
NM_004588.5(SCN2B):c.116A>G (p.Asn39Ser)
NM_004588.5(SCN2B):c.125A>G (p.Asn42Ser) rs2135518443
NM_004588.5(SCN2B):c.139C>T (p.Arg47Cys)
NM_004588.5(SCN2B):c.145C>T (p.Pro49Ser)
NM_004588.5(SCN2B):c.154T>C (p.Phe52Leu) rs1948405888
NM_004588.5(SCN2B):c.191C>T (p.Ser64Phe)
NM_004588.5(SCN2B):c.25C>T (p.Arg9Cys) rs878854711
NM_004588.5(SCN2B):c.267C>G (p.Asn89Lys) rs2135518217
NM_004588.5(SCN2B):c.274C>G (p.Leu92Val)
NM_004588.5(SCN2B):c.28C>T (p.Pro10Ser)
NM_004588.5(SCN2B):c.290A>G (p.Asp97Gly)
NM_004588.5(SCN2B):c.292C>G (p.Arg98Gly) rs771234231
NM_004588.5(SCN2B):c.295G>T (p.Val99Leu) rs772817742
NM_004588.5(SCN2B):c.299A>G (p.Glu100Gly) rs552421963
NM_004588.5(SCN2B):c.325G>A (p.Asp109Asn)
NM_004588.5(SCN2B):c.338T>C (p.Met113Thr)
NM_004588.5(SCN2B):c.344G>A (p.Arg115Lys) rs750313446
NM_004588.5(SCN2B):c.346A>G (p.Asn116Asp)
NM_004588.5(SCN2B):c.367G>A (p.Gly123Arg)
NM_004588.5(SCN2B):c.388A>T (p.Met130Leu) rs1316023322
NM_004588.5(SCN2B):c.412G>A (p.Gly138Ser) rs1948399832
NM_004588.5(SCN2B):c.419G>A (p.Gly140Asp)
NM_004588.5(SCN2B):c.420C>T (p.Gly140=)
NM_004588.5(SCN2B):c.446A>G (p.Glu149Gly)
NM_004588.5(SCN2B):c.448+6G>C rs1948399268
NM_004588.5(SCN2B):c.449-2A>C rs1085307094
NM_004588.5(SCN2B):c.452C>A (p.Pro151His) rs765701955
NM_004588.5(SCN2B):c.457G>A (p.Glu153Lys)
NM_004588.5(SCN2B):c.490G>A (p.Ala164Thr)
NM_004588.5(SCN2B):c.502G>T (p.Gly168Cys)
NM_004588.5(SCN2B):c.522C>G (p.Ile174Met)
NM_004588.5(SCN2B):c.53G>A (p.Ser18Asn)
NM_004588.5(SCN2B):c.554G>C (p.Arg185Thr)
NM_004588.5(SCN2B):c.563A>G (p.Glu188Gly) rs1948388818
NM_004588.5(SCN2B):c.573del (p.Ser192fs)
NM_004588.5(SCN2B):c.578C>G (p.Thr193Arg) rs115353159
NM_004588.5(SCN2B):c.578C>T (p.Thr193Ile)
NM_004588.5(SCN2B):c.616G>A (p.Gly206Ser) rs1591444155
NM_004588.5(SCN2B):c.622G>A (p.Gly208Ser) rs1024654954
NM_004588.5(SCN2B):c.625_626delinsCC (p.Asn209Pro) rs1064796044
NM_004588.5(SCN2B):c.71-1G>A
NM_004588.5(SCN2B):c.86G>A (p.Ser29Asn)

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