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

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002890.3(RASA1):c.239C>T (p.Ala80Val)	rs764720303
NM_002890.3(RASA1):c.334G>A (p.Gly112Arg)	rs2112222851
NM_002890.3(RASA1):c.539+298G>A

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