ClinVar Miner

List of variants in gene CACNA1C studied for cardiac conduction defect

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000719.7(CACNA1C):c.32del (p.Pro11fs)	rs2052999161
NM_000719.7(CACNA1C):c.5626A>G (p.Lys1876Glu)	rs869025368
NM_000719.7(CACNA1C):c.985G>A (p.Gly329Ser)	rs786205744

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