ClinVar Miner

List of variants reported as likely benign for cerebral cavernous malformation by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_031443.4(CCM2):c.980A>G (p.Asn327Ser)	rs150428392	0.00128
NM_031443.4(CCM2):c.1217C>T (p.Thr406Met)	rs150734280	0.00119
NM_031443.4(CCM2):c.48A>T (p.Pro16=)	rs142320735	0.00003

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