List of variants in gene CACNA1A reported as benign for cardiovascular disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.1987-98C>T	rs4926263	0.99259
NM_001127222.2(CACNA1A):c.6526+137A>G	rs10413221	0.98446
NM_001127222.2(CACNA1A):c.4950+96A>C	rs16039	0.97758
NM_001127222.2(CACNA1A):c.1199-31A>G	rs16008	0.81362
NM_001127222.2(CACNA1A):c.5941-205T>C	rs2419233	0.76943
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.1198+48G>A	rs2306348	0.64420
NM_001127222.2(CACNA1A):c.1182G>A (p.Glu394=)	rs2248069	0.64010
NM_001127222.2(CACNA1A):c.4867-71A>C	rs16035	0.59301
NM_001127222.2(CACNA1A):c.5731+49C>T	rs3816027	0.54210
NM_001127222.2(CACNA1A):c.4089+71T>C	rs16031	0.53636
NM_001127222.2(CACNA1A):c.293+53G>A	rs16003	0.45781
NM_001127222.2(CACNA1A):c.2280-68C>A	rs12985136	0.45430
NM_001127222.2(CACNA1A):c.4756-97G>A	rs8103699	0.24285
NM_001127222.2(CACNA1A):c.6378C>T (p.Ser2126=)	rs16050	0.02098
NM_001127222.2(CACNA1A):c.3546C>T (p.Val1182=)	rs16029	0.01749
NM_001127222.2(CACNA1A):c.5739C>T (p.Ala1913=)	rs16044	0.01420
NM_001127222.2(CACNA1A):c.462C>T (p.Ala154=)	rs1800039	0.00699
NM_001127222.2(CACNA1A):c.1345+7C>T	rs192536793	0.00213
NM_001127222.2(CACNA1A):c.5625+50CTT[4]	rs143245670
NM_001127222.2(CACNA1A):c.6189+74A>C	rs16048
NM_001127222.2(CACNA1A):c.6303+94del	rs3217380
NM_001127222.2(CACNA1A):c.6526+124G>C	rs2304093

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