Disease: LEOPARD SYNDROME 3 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906661
rs387906661
Entrez Id: 673
Gene Symbol: BRAF
BRAF
CUI: C3150971
Disease:
LEOPARD SYNDROME 3 		0.800 GeneticVariation UNIPROT Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169 2009
dbSNP: rs387906661
rs387906661
Entrez Id: 673
Gene Symbol: BRAF
BRAF
CUI: C3150971
Disease:
LEOPARD SYNDROME 3 		G 0.800 CausalMutation CLINVAR
dbSNP: rs180177042
rs180177042
Entrez Id: 673
Gene Symbol: BRAF
BRAF
CUI: C3150971
Disease:
LEOPARD SYNDROME 3 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs387906660
rs387906660
Entrez Id: 673
Gene Symbol: BRAF
BRAF
CUI: C3150971
Disease:
LEOPARD SYNDROME 3 		A 0.700 CausalMutation CLINVAR
dbSNP: rs397507466
rs397507466
Entrez Id: 673
Gene Symbol: BRAF
BRAF
CUI: C3150971
Disease:
LEOPARD SYNDROME 3 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs397507466
rs397507466
Entrez Id: 673
Gene Symbol: BRAF
BRAF
CUI: C3150971
Disease:
LEOPARD SYNDROME 3 		G 0.700 CausalMutation CLINVAR
dbSNP: rs397516895
rs397516895
Entrez Id: 673
Gene Symbol: BRAF
BRAF
CUI: C3150971
Disease:
LEOPARD SYNDROME 3 		T 0.700 GeneticVariation CLINVAR