Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113488022
rs113488022
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
T 0.900 CausalMutation CLINVAR

dbSNP: rs121913279
rs121913279
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
G 0.820 CausalMutation CLINVAR

dbSNP: rs387906555
rs387906555
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs387906555
rs387906555
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR

dbSNP: rs28937578
rs28937578
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs28937578
rs28937578
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR

dbSNP: rs281865417
rs281865417
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR

dbSNP: rs267606892
rs267606892
ND3 ; ND4 ; ND4L ; ND5
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs267606892
rs267606892
ND3 ; ND4 ; ND4L ; ND5
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.800 CausalMutation CLINVAR

dbSNP: rs267606884
rs267606884
ATP6 ; ATP8 ; COX1 ; COX2 ; COX3
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.800 CausalMutation CLINVAR

dbSNP: rs207459996
rs207459996
CYTB ; ND6
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs207459996
rs207459996
CYTB ; ND6
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.800 CausalMutation CLINVAR

dbSNP: rs199474826
rs199474826
ATP6 ; ATP8 ; COX2 ; COX3
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs199474826
rs199474826
ATP6 ; ATP8 ; COX2 ; COX3
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR

dbSNP: rs180177033
rs180177033
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.800 CausalMutation CLINVAR

dbSNP: rs180177032
rs180177032
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR

dbSNP: rs137853148
rs137853148
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
T 0.800 CausalMutation CLINVAR

dbSNP: rs121917732
rs121917732
MCC
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs121917732
rs121917732
MCC
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
T 0.800 CausalMutation CLINVAR

dbSNP: rs121917731
rs121917731
MCC
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR

dbSNP: rs121917731
rs121917731
MCC
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs121913529
rs121913529
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 GeneticVariation UNIPROT

dbSNP: rs121913400
rs121913400
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR

dbSNP: rs121913364
rs121913364
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.800 CausalMutation CLINVAR

dbSNP: rs121913348
rs121913348
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
T 0.800 CausalMutation CLINVAR