ClinVar Miner

List of variants in gene SCN5A reported as uncertain significance for Sick sinus syndrome

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP
NM_000335.4(SCN5A):c.2436+12G>A rs41312419
NM_001099404.1(SCN5A):c.1598G>A (p.Arg533His) rs146848219
NM_001099404.1(SCN5A):c.4267G>A (p.Asp1423Asn) rs746291609
NM_198056.2(SCN5A):c.*1048G>A rs886058447
NM_198056.2(SCN5A):c.*1074C>G rs776171341
NM_198056.2(SCN5A):c.*1087G>A rs886058446
NM_198056.2(SCN5A):c.*1164G>T rs41315489
NM_198056.2(SCN5A):c.*1390A>G rs41310753
NM_198056.2(SCN5A):c.*1443C>A rs886058445
NM_198056.2(SCN5A):c.*1496T>G rs41313015
NM_198056.2(SCN5A):c.*1568G>C rs45503498
NM_198056.2(SCN5A):c.*1602G>T rs886058444
NM_198056.2(SCN5A):c.*160G>A rs772585696
NM_198056.2(SCN5A):c.*1673C>T rs886058443
NM_198056.2(SCN5A):c.*1691G>T rs886058442
NM_198056.2(SCN5A):c.*1701G>T rs886058441
NM_198056.2(SCN5A):c.*1705C>T rs886058440
NM_198056.2(SCN5A):c.*1731G>C rs569249327
NM_198056.2(SCN5A):c.*1744C>G rs886058439
NM_198056.2(SCN5A):c.*1836A>T rs886058438
NM_198056.2(SCN5A):c.*1932C>T rs886058437
NM_198056.2(SCN5A):c.*1943C>A rs569552176
NM_198056.2(SCN5A):c.*1969C>T rs190416544
NM_198056.2(SCN5A):c.*204T>C rs147795595
NM_198056.2(SCN5A):c.*2135C>A rs45502793
NM_198056.2(SCN5A):c.*2149G>A rs114517792
NM_198056.2(SCN5A):c.*290G>A rs886058457
NM_198056.2(SCN5A):c.*296G>A rs886058456
NM_198056.2(SCN5A):c.*331T>C rs551399685
NM_198056.2(SCN5A):c.*382T>C rs45459402
NM_198056.2(SCN5A):c.*486C>T rs886058455
NM_198056.2(SCN5A):c.*516G>T rs886058454
NM_198056.2(SCN5A):c.*634C>A rs886058453
NM_198056.2(SCN5A):c.*663C>A rs540984871
NM_198056.2(SCN5A):c.*677G>A rs45458203
NM_198056.2(SCN5A):c.*6G>T rs776980213
NM_198056.2(SCN5A):c.*705C>A rs886058452
NM_198056.2(SCN5A):c.*725C>A rs886058451
NM_198056.2(SCN5A):c.*73C>A rs886058458
NM_198056.2(SCN5A):c.*747G>A rs763830252
NM_198056.2(SCN5A):c.*889C>A rs546849670
NM_198056.2(SCN5A):c.*920G>C rs561475141
NM_198056.2(SCN5A):c.*945C>A rs886058450
NM_198056.2(SCN5A):c.*980C>A rs886058449
NM_198056.2(SCN5A):c.*990T>C rs886058448
NM_198056.2(SCN5A):c.-107G>A rs886058466
NM_198056.2(SCN5A):c.-53+12C>T rs886058464
NM_198056.2(SCN5A):c.-70C>T rs886058465
NM_198056.2(SCN5A):c.1044C>T (p.Pro348=) rs370346797
NM_198056.2(SCN5A):c.1068T>C (p.Asp356=) rs41313703
NM_198056.2(SCN5A):c.1491T>G (p.Ser497=) rs761505485
NM_198056.2(SCN5A):c.1569T>A (p.Arg523=) rs41313693
NM_198056.2(SCN5A):c.1681C>T (p.Leu561=) rs45522138
NM_198056.2(SCN5A):c.1743G>A (p.Ser581=) rs41313687
NM_198056.2(SCN5A):c.1800G>A (p.Val600=) rs758101066
NM_198056.2(SCN5A):c.1870C>A (p.Leu624Ile) rs886058463
NM_198056.2(SCN5A):c.2151G>A (p.Pro717=) rs191840835
NM_198056.2(SCN5A):c.2181C>T (p.Ile727=) rs186942072
NM_198056.2(SCN5A):c.21T>A (p.Pro7=) rs587781157
NM_198056.2(SCN5A):c.2259C>T (p.Asn753=) rs878911306
NM_198056.2(SCN5A):c.2437-5C>A rs72549411
NM_198056.2(SCN5A):c.3391-7T>C rs41310769
NM_198056.2(SCN5A):c.3463C>T (p.Pro1155Ser) rs781103369
NM_198056.2(SCN5A):c.3542T>C (p.Val1181Ala) rs376965389
NM_198056.2(SCN5A):c.3873G>A (p.Leu1291=) rs41313033
NM_198056.2(SCN5A):c.4109A>G (p.Asp1370Gly) rs775485359
NM_198056.2(SCN5A):c.4437+13C>T rs148598985
NM_198056.2(SCN5A):c.4671C>T (p.Ile1557=) rs886058461
NM_198056.2(SCN5A):c.4824C>T (p.Leu1608=) rs45437099
NM_198056.2(SCN5A):c.4827G>A (p.Ser1609=) rs886058460
NM_198056.2(SCN5A):c.5286C>T (p.Ile1762=) rs375323548
NM_198056.2(SCN5A):c.5454C>T (p.Ala1818=) rs370114378
NM_198056.2(SCN5A):c.5607C>T (p.Asp1869=) rs560476223
NM_198056.2(SCN5A):c.5945G>T (p.Arg1982Ile) rs774432823
NM_198056.2(SCN5A):c.5971C>T (p.Arg1991Trp) rs371308670
NM_198056.2(SCN5A):c.6003C>T (p.Leu2001=) rs538707712
NM_198056.2(SCN5A):c.6033C>A (p.Asp2011Glu) rs886058459
NM_198056.2(SCN5A):c.687T>C (p.Thr229=) rs770390440
NM_198056.2(SCN5A):c.787G>A (p.Val263Ile) rs752824646

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