Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs749415085
rs749415085
0.807 0.160 3 179198937 missense variant C/A;G;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs749415085
rs749415085
0.807 0.160 3 179198937 missense variant C/A;G;T snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.700 1.000 1 2016 2016
dbSNP: rs749415085
rs749415085
0.807 0.160 3 179198937 missense variant C/A;G;T snv
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs749415085
rs749415085
0.807 0.160 3 179198937 missense variant C/A;G;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs749415085
rs749415085
0.807 0.160 3 179198937 missense variant C/A;G;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs749415085
rs749415085
0.807 0.160 3 179198937 missense variant C/A;G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs749415085
rs749415085
0.807 0.160 3 179198937 missense variant C/A;G;T snv
Malignant neoplasm of large intestine
0.700 0