List of variants in gene combination CACNA1A, LOC108663985 reported as benign by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.6937CAG[11] (p.Gln2324_Gln2325del)	rs16054
NM_001127222.2(CACNA1A):c.6937CAG[12] (p.Gln2325del)	rs16054
NM_001127222.2(CACNA1A):c.6937CAG[14] (p.Gln2325dup)	rs16054
NM_001127222.2(CACNA1A):c.6937CAG[4] (p.Gln2317_Gln2325del)	rs16054
NM_001127222.2(CACNA1A):c.6937CAG[7] (p.Gln2320_Gln2325del)	rs16054

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