Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906661
rs387906661
BRAF
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs397507466
rs397507466
BRAF
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		A 0.700 CausalMutation CLINVAR