ClinVar Miner

List of variants reported as likely benign for atrial fibrillation (disease) by Invitae

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_001002841.1(MYL4):c.313+8C>A rs372826462
NM_001002841.1(MYL4):c.522G>A (p.Leu174=) rs767533462
NM_001002841.1(MYL4):c.537G>A (p.Glu179=) rs181540609
NM_002234.4(KCNA5):c.1114C>T (p.Leu372=) rs1047059016
NM_002234.4(KCNA5):c.1539C>T (p.Pro513=) rs145832242
NM_002234.4(KCNA5):c.1595C>T (p.Pro532Leu) rs17221812
NM_002234.4(KCNA5):c.1672G>A (p.Gly558Arg) rs201328038
NM_002234.4(KCNA5):c.213_245del (p.Asp72_Pro82del) rs144879674
NM_002234.4(KCNA5):c.221G>A (p.Gly74Glu) rs555008698
NM_002234.4(KCNA5):c.36T>G (p.Gly12=) rs886049572
NM_002234.4(KCNA5):c.464A>G (p.Tyr155Cys) rs202117321
NM_002234.4(KCNA5):c.633G>C (p.Glu211Asp) rs35853292
NM_002234.4(KCNA5):c.634C>T (p.Arg212Cys) rs77281462
NM_002234.4(KCNA5):c.816G>A (p.Leu272=) rs775088698
NM_002234.4(KCNA5):c.898G>A (p.Gly300Ser) rs148708451
NM_002234.4(KCNA5):c.919C>T (p.Pro307Ser) rs17215409
NM_002234.4(KCNA5):c.92G>T (p.Gly31Val) rs61737395
NM_002234.4(KCNA5):c.961G>A (p.Ala321Thr) rs765142607
NM_002476.2(MYL4):c.167T>C (p.Phe56Ser) rs144870368
NM_002476.2(MYL4):c.405C>T (p.Phe135=) rs150593274
NM_004588.5(SCN2B):c.150C>T (p.Cys50=) rs751437266
NM_004588.5(SCN2B):c.238-6C>T rs200842493
NM_004588.5(SCN2B):c.615C>T (p.Asp205=) rs201971719
NM_006172.4(NPPA):c.135C>T (p.Asp45=) rs148712945
NM_006172.4(NPPA):c.171C>T (p.Val57=) rs61757262
NM_006172.4(NPPA):c.190A>C (p.Ser64Arg) rs61757261
NM_006172.4(NPPA):c.198G>A (p.Pro66=) rs767807184
NM_006172.4(NPPA):c.252C>T (p.Thr84=) rs755212754
NM_006172.4(NPPA):c.292G>A (p.Gly98Arg) rs142022010
NM_006172.4(NPPA):c.83T>C (p.Met28Thr) rs142116829

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