ClinVar Miner

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

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_002234.4(KCNA5):c.1020C>T (p.Leu340=) rs72546671
NM_002234.4(KCNA5):c.1149_1150inv (p.Gly384Arg)
NM_002234.4(KCNA5):c.1353C>T (p.Ala451=) rs767826909
NM_002234.4(KCNA5):c.1497G>A (p.Leu499=) rs17221805
NM_002234.4(KCNA5):c.1733G>A (p.Arg578Lys) rs12720445
NM_002234.4(KCNA5):c.180G>A (p.Ala60=) rs376660949
NM_002234.4(KCNA5):c.229C>T (p.Pro77Ser) rs202083721
NM_002234.4(KCNA5):c.381C>T (p.Ser127=) rs45504599
NM_002234.4(KCNA5):c.570C>T (p.Asn190=) rs12720444
NM_002234.4(KCNA5):c.615G>C (p.Leu205=) rs12720443
NM_002234.4(KCNA5):c.751G>A (p.Ala251Thr) rs12720442
NM_002234.4(KCNA5):c.929C>T (p.Pro310Leu) rs17215402
NM_002476.2(MYL4):c.150C>T (p.Ala50=) rs143234546
NM_002476.2(MYL4):c.314-4G>A rs114024716
NM_002476.2(MYL4):c.488-4G>A rs146859926
NM_002476.2(MYL4):c.488-5C>T rs376118927
NM_002476.2(MYL4):c.556A>T (p.Asn186Tyr) rs16941677
NM_004588.5(SCN2B):c.498C>T (p.Val166=) rs200709238
NM_181703.4(GJA5):c.369C>T (p.Tyr123=) rs2232191

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