List of variants in gene CACNA1C reported as uncertain significance by ISCA site 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 12p13.33(chr12:2564298-2674054)x3
GRCh37/hg19 12p13.33(chr12:2796406-2844076)x3
GRCh37/hg19 12p13.33(chr12:2796406-2851026)x1

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