List of variants in gene CACNA1A reported as uncertain significance by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.2804G>A (p.Arg935Gln)	rs768048563	0.00003
NM_001127222.2(CACNA1A):c.6647A>C (p.His2216Pro)	rs2054687187	0.00002
NM_001127222.2(CACNA1A):c.1166T>C (p.Leu389Pro)	rs2058520816
NM_001127222.2(CACNA1A):c.1555+3_1555+6del	rs2058143459
NM_001127222.2(CACNA1A):c.3692+1G>A	rs1315533129
NM_001127222.2(CACNA1A):c.4089+18T>G	rs1600198282

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