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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002890.3(RASA1):c.346C>G (p.Leu116Val)	rs149246093	0.00006
NM_002890.3(RASA1):c.539+298G>A	rs778752048	0.00003
NM_002890.3(RASA1):c.239C>T (p.Ala80Val)	rs764720303	0.00001
NM_002890.3(RASA1):c.2462T>A (p.Ile821Lys)	rs2112495755
NM_002890.3(RASA1):c.334G>A (p.Gly112Arg)	rs2112222851

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