ClinVar Miner

List of variants reported as likely pathogenic for atrial fibrillation by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (51):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_002476.2(MYL4):c.487+1G>A rs769405762 0.00001
NM_002476.2(MYL4):c.488-1G>A rs770372675 0.00001
NM_002476.2(MYL4):c.135+1G>A
NM_002476.2(MYL4):c.164-1G>C
NM_002476.2(MYL4):c.313+1G>T
NM_002476.2(MYL4):c.314-1G>C
NM_002476.2(MYL4):c.487+1G>C rs769405762

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