List of variants in gene CACNA1A reported as uncertain significance by Clinical Genetics Laboratory, Skane University Hospital Lund

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.3533T>A (p.Leu1178His)	rs761259850	0.00003
NM_001127222.2(CACNA1A):c.6647_6658del (p.His2216_His2219del)	rs770368215

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