Gene: BRAF ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913369
rs121913369
BRAF
C 0.800 CausalMutation CLINVAR

dbSNP: rs606231228
rs606231228
BRAF
G 0.800 CausalMutation CLINVAR

dbSNP: rs387906660
rs387906660
BRAF
A 0.700 GeneticVariation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs1562957000
rs1562957000
BRAF
C 0.700 GeneticVariation CLINVAR

dbSNP: rs180177042
rs180177042
BRAF
T 0.700 GeneticVariation CLINVAR

dbSNP: rs387906660
rs387906660
BRAF
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906660
rs387906660
BRAF
C 0.700 CausalMutation CLINVAR

dbSNP: rs387906661
rs387906661
BRAF
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507466
rs397507466
BRAF
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397516895
rs397516895
BRAF
T 0.700 GeneticVariation CLINVAR