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

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Show significances as they were submitted (without aggregation into standard terms)
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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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