ClinVar Miner

List of variants in gene CCM2 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_031443.4(CCM2):c.920G>A (p.Arg307His)	rs372739455	0.00004
NM_031443.4(CCM2):c.1120G>A (p.Val374Met)	rs200669376
NM_031443.4(CCM2):c.44C>T (p.Ser15Leu)

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