List of variants in gene CACNA1A reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.6657T>C (p.His2219=)	rs16051	0.67380
NM_001127222.2(CACNA1A):c.2173-12C>T	rs16018	0.66161
NM_001127222.2(CACNA1A):c.3057G>A (p.Arg1019=)	rs16025	0.14118
NM_001127222.2(CACNA1A):c.2975A>T (p.Glu992Val)	rs16023	0.13336
NM_001127222.2(CACNA1A):c.2751G>C (p.Glu917Asp)	rs16022	0.11855
NM_001127222.2(CACNA1A):c.3310G>A (p.Gly1104Ser)	rs16027	0.07737
NM_001127222.2(CACNA1A):c.6837G>A (p.Pro2279=)	rs147221323	0.03348
NM_001127222.2(CACNA1A):c.3546C>T (p.Val1182=)	rs16029	0.01749
NM_001127222.2(CACNA1A):c.1776C>G (p.Val592=)	rs16012	0.01217
NM_001127222.2(CACNA1A):c.6126G>A (p.Thr2042=)	rs7249722	0.00766
NM_001127222.2(CACNA1A):c.3237C>T (p.Ala1079=)	rs16026	0.00616
NM_001127222.2(CACNA1A):c.3040G>A (p.Glu1014Lys)	rs16024	0.00390
NM_001127222.2(CACNA1A):c.1345+7C>T	rs192536793	0.00213

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