ClinVar Miner

List of variants reported as likely benign for Basal cell carcinoma, susceptibility to, 1; Capillary malformation-arteriovenous malformation 1

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002890.3(RASA1):c.296C>T (p.Ala99Val)	rs111840875	0.02050
NM_002890.3(RASA1):c.360C>A (p.Pro120=)	rs137878395	0.00061
NM_002890.3(RASA1):c.1209A>G (p.Pro403=)	rs367991324	0.00009

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