List of variants in gene combination CACNA1A, LOC130063717 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.6760G>C (p.Glu2254Gln)	rs779063280	0.00014
NM_001127222.2(CACNA1A):c.6731G>A (p.Arg2244His)	rs1057521565	0.00004
NM_001127222.2(CACNA1A):c.6769G>A (p.Ala2257Thr)	rs1057523197	0.00001
NM_001127222.2(CACNA1A):c.6774C>T (p.His2258=)	rs766371895
NM_001127222.2(CACNA1A):c.6775C>A (p.Arg2259=)	rs750267834

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