List of variants in gene combination CCNH, RASA1 reported as pathogenic for Basal cell carcinoma, susceptibility to, 1; Capillary malformation-arteriovenous malformation 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002890.3(RASA1):c.2245C>T (p.Arg749Ter)	rs1204340475	0.00001
NM_002890.3(RASA1):c.2131C>T (p.Arg711Ter)	rs863223718
NM_002890.3(RASA1):c.3055C>T (p.Gln1019Ter)	rs1060503440
NM_002890.3(RASA1):c.613_617del (p.Leu205fs)	rs1060503441
NM_002890.3(RASA1):c.656C>G (p.Ser219Ter)	rs1554044823

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