Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906660
rs387906660
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507477
rs397507477
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397509343
rs397509343
C 0.700 GeneticVariation CLINVAR

dbSNP: rs397516891
rs397516891
C 0.700 GeneticVariation CLINVAR

dbSNP: rs397516903
rs397516903
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397516903
rs397516903
C 0.700 GeneticVariation CLINVAR

dbSNP: rs397516904
rs397516904
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397516905
rs397516905
G 0.700 GeneticVariation CLINVAR

dbSNP: rs727502904
rs727502904
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727504375
rs727504375
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121913348
rs121913348
T 0.700 GeneticVariation CLINVAR Mutations of the BRAF gene in cholangiocarcinoma but not in hepatocellular carcinoma. 12692057

2003

dbSNP: rs121913369
rs121913369
C 0.700 CausalMutation CLINVAR Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. 15035987

2004

dbSNP: rs180177034
rs180177034
G 0.700 CausalMutation CLINVAR Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome. 16474404

2006

dbSNP: rs180177036
rs180177036
G 0.700 CausalMutation CLINVAR Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome. 16474404

2006

dbSNP: rs180177036
rs180177036
G 0.700 CausalMutation CLINVAR Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome. 16439621

2006

dbSNP: rs180177036
rs180177036
A 0.700 CausalMutation CLINVAR Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome. 16474404

2006

dbSNP: rs180177036
rs180177036
A 0.700 CausalMutation CLINVAR Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome. 16439621

2006

dbSNP: rs180177038
rs180177038
T 0.700 CausalMutation CLINVAR Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome. 16474404

2006

dbSNP: rs180177038
rs180177038
T 0.700 CausalMutation CLINVAR Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome. 16439621

2006

dbSNP: rs397507483
rs397507483
A 0.700 CausalMutation CLINVAR Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome. 16439621

2006

dbSNP: rs121913348
rs121913348
T 0.700 GeneticVariation CLINVAR Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome. 17704260

2007

dbSNP: rs121913348
rs121913348
T 0.700 GeneticVariation CLINVAR Mutation analysis of BRAF, MEK1 and MEK2 in 15 ovarian cancer cell lines: implications for therapy. 18060073

2007

dbSNP: rs121913364
rs121913364
G 0.700 CausalMutation CLINVAR KRAS and BRAF oncogenic mutations in MSS colorectal carcinoma progression. 16953233

2007

dbSNP: rs180177034
rs180177034
G 0.700 CausalMutation CLINVAR Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome. 17704260

2007

dbSNP: rs180177036
rs180177036
A 0.700 CausalMutation CLINVAR Neurological complications of cardio-facio-cutaneous syndrome. 18039235

2007