List of variants in gene CALHM3 reported as likely benign

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001129742.2(CALHM3):c.253G>T (p.Ala85Ser)
NM_001129742.2(CALHM3):c.581C>T (p.Ala194Val)
NM_001129742.2(CALHM3):c.836G>T (p.Gly279Val)

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