List of variants in gene CCM2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_031443.4(CCM2):c.246C>T (p.Pro82=)	rs148244188	0.00183
NM_031443.4(CCM2):c.980A>G (p.Asn327Ser)	rs150428392	0.00128
NM_031443.4(CCM2):c.339C>T (p.Leu113=)	rs146259619	0.00032
NM_031443.4(CCM2):c.126G>A (p.Leu42=)	rs146579519	0.00021
NM_031443.4(CCM2):c.1164C>T (p.His388=)
NM_031443.4(CCM2):c.1326C>T (p.Asp442=)

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