List of variants in gene CACNA1C reported as benign by PreventionGenetics, part of Exact Sciences

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000719.7(CACNA1C):c.5361G>A (p.Thr1787=)	rs1051375	0.57002
NM_000719.7(CACNA1C):c.617+19T>C	rs1544516	0.27158
NM_000719.7(CACNA1C):c.617+17G>A	rs1544515	0.27035
NM_000719.7(CACNA1C):c.3786C>T (p.Phe1262=)	rs216008	0.20673
NM_000719.7(CACNA1C):c.522G>A (p.Ala174=)	rs1544514	0.16949
NM_000719.7(CACNA1C):c.4038C>T (p.Ile1346=)	rs56180838	0.04572
NM_000719.7(CACNA1C):c.5292C>T (p.Asn1764=)	rs72552065	0.04512
NM_000719.7(CACNA1C):c.372-15G>A	rs55792866	0.02977
NM_000719.7(CACNA1C):c.5383G>A (p.Gly1795Arg)	rs111298509	0.01614
NM_000719.7(CACNA1C):c.171C>T (p.Asp57=)	rs34419050	0.01584
NM_000719.7(CACNA1C):c.3387G>A (p.Thr1129=)	rs188224114	0.00525
NM_000719.7(CACNA1C):c.2449C>T (p.Pro817Ser)	rs112532048	0.00279
NM_000719.7(CACNA1C):c.5665C>T (p.Arg1889Cys)	rs185788586	0.00182
NM_000719.7(CACNA1C):c.5918G>A (p.Arg1973Gln)	rs112414325	0.00140
NM_000719.7(CACNA1C):c.3780C>A (p.Gly1260=)	rs201258230	0.00131
NM_000719.7(CACNA1C):c.3049-10C>T	rs186741807	0.00093
NM_000719.7(CACNA1C):c.5445-585G>A	rs113722042

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