Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113488022
rs113488022
BRAF
T 0.900 CausalMutation CLINVAR

dbSNP: rs121913279
rs121913279
PIK3CA
G 0.820 CausalMutation CLINVAR

dbSNP: rs104886003
rs104886003
PIK3CA
A 0.800 CausalMutation CLINVAR

dbSNP: rs121434595
rs121434595
NRAS
0.800 GeneticVariation UNIPROT

dbSNP: rs121434595
rs121434595
NRAS
G 0.800 CausalMutation CLINVAR

dbSNP: rs121913111
rs121913111
FGFR3
0.800 GeneticVariation UNIPROT

dbSNP: rs121913111
rs121913111
FGFR3
A 0.800 CausalMutation CLINVAR

dbSNP: rs121913348
rs121913348
BRAF
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913364
rs121913364
BRAF
C 0.800 CausalMutation CLINVAR

dbSNP: rs121913400
rs121913400
CTNNB1
A 0.800 CausalMutation CLINVAR

dbSNP: rs121913529
rs121913529
KRAS
0.800 GeneticVariation UNIPROT

dbSNP: rs121917731
rs121917731
MCC
A 0.800 CausalMutation CLINVAR

dbSNP: rs121917731
rs121917731
MCC
0.800 GeneticVariation UNIPROT

dbSNP: rs121917732
rs121917732
MCC
0.800 GeneticVariation UNIPROT

dbSNP: rs121917732
rs121917732
MCC
T 0.800 CausalMutation CLINVAR

dbSNP: rs137853148
rs137853148
PDGFRL
T 0.800 CausalMutation CLINVAR

dbSNP: rs180177032
rs180177032
BRAF
A 0.800 CausalMutation CLINVAR

dbSNP: rs180177033
rs180177033
BRAF
C 0.800 CausalMutation CLINVAR

dbSNP: rs199474826
rs199474826
ATP6 ; ATP8 ; COX2 ; COX3
0.800 GeneticVariation UNIPROT

dbSNP: rs199474826
rs199474826
ATP6 ; ATP8 ; COX2 ; COX3
A 0.800 CausalMutation CLINVAR

dbSNP: rs207459996
rs207459996
CYTB ; ND6
0.800 GeneticVariation UNIPROT

dbSNP: rs207459996
rs207459996
CYTB ; ND6
C 0.800 CausalMutation CLINVAR

dbSNP: rs267606884
rs267606884
ATP6 ; ATP8 ; COX1 ; COX2 ; COX3
C 0.800 CausalMutation CLINVAR

dbSNP: rs267606892
rs267606892
ND3 ; ND4 ; ND4L ; ND5
0.800 GeneticVariation UNIPROT

dbSNP: rs267606892
rs267606892
ND3 ; ND4 ; ND4L ; ND5
C 0.800 CausalMutation CLINVAR