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: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.710 0.500 1 2009 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
Transitional cell carcinoma of bladder
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
0.732 0.320 17 7674237 missense variant G/A;C snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.700 1.000 1 2016 2016