Gene: BRAF ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177035
rs180177035
BRAF
C 0.700 CausalMutation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs180177040
rs180177040
BRAF
C 0.700 CausalMutation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs180177041
rs180177041
BRAF
G 0.700 GeneticVariation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs180177042
rs180177042
BRAF
T 0.700 GeneticVariation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs387906660
rs387906660
BRAF
C 0.700 CausalMutation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs397507469
rs397507469
BRAF
T 0.700 GeneticVariation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs397516893
rs397516893
BRAF
C 0.700 CausalMutation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs869025340
rs869025340
BRAF
T 0.700 CausalMutation CLINVAR The RASopathies. 23875798

2013
dbSNP: rs180177035
rs180177035
BRAF
C 0.700 CausalMutation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs180177040
rs180177040
BRAF
C 0.700 CausalMutation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs180177041
rs180177041
BRAF
G 0.700 GeneticVariation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs180177042
rs180177042
BRAF
T 0.700 GeneticVariation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs387906660
rs387906660
BRAF
C 0.700 CausalMutation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs397507469
rs397507469
BRAF
T 0.700 GeneticVariation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs397516893
rs397516893
BRAF
C 0.700 CausalMutation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs869025340
rs869025340
BRAF
T 0.700 CausalMutation CLINVAR Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. 19206169

2009
dbSNP: rs180177035
rs180177035
BRAF
C 0.700 CausalMutation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs180177040
rs180177040
BRAF
C 0.700 CausalMutation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs180177041
rs180177041
BRAF
G 0.700 GeneticVariation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs180177042
rs180177042
BRAF
T 0.700 GeneticVariation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs387906660
rs387906660
BRAF
C 0.700 CausalMutation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs397507469
rs397507469
BRAF
T 0.700 GeneticVariation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs397516893
rs397516893
BRAF
C 0.700 CausalMutation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs869025340
rs869025340
BRAF
T 0.700 CausalMutation CLINVAR Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. 18413255

2008
dbSNP: rs180177035
rs180177035
BRAF
C 0.700 CausalMutation CLINVAR Neurological complications of cardio-facio-cutaneous syndrome. 18039235

2007