List of variants in gene CACNA1A reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.5650G>A (p.Val1884Ile)	rs201836062	0.00070
NM_001127222.2(CACNA1A):c.888C>T (p.Asn296=)	rs372812865	0.00026
NM_001127222.2(CACNA1A):c.6527-16C>T	rs752985059	0.00007
NM_001127222.2(CACNA1A):c.2501A>C (p.Asn834Thr)	rs201666606	0.00006
NM_001127222.2(CACNA1A):c.633T>C (p.Ser211=)	rs202216404	0.00005
NM_001127222.2(CACNA1A):c.219G>C (p.Thr73=)	rs781239273	0.00004
NM_001127222.2(CACNA1A):c.2692G>A (p.Gly898Ser)	rs751726770	0.00004
NM_001127222.2(CACNA1A):c.1990C>T (p.Leu664=)	rs1246140836	0.00003
NM_001127222.2(CACNA1A):c.540-20T>C	rs756413933	0.00002
NM_001127222.2(CACNA1A):c.6464G>T (p.Arg2155Leu)	rs572722130	0.00002
NM_001127222.2(CACNA1A):c.2289A>G (p.Gln763=)	rs771044445	0.00001
NM_001127222.2(CACNA1A):c.6303+14C>T	rs777901156	0.00001
NM_001127222.2(CACNA1A):c.6705C>T (p.His2235=)	rs1376732755	0.00001
NM_001127222.2(CACNA1A):c.5401-10G>T	rs370129945
NM_001127222.2(CACNA1A):c.5820G>A (p.Leu1940=)

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