Source: ALL

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: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
Liver and Intrahepatic Biliary Tract Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0003164
Disease: Anthracosilicosis
Anthracosilicosis
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.010 < 0.001 1 2018 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease
0.010 1.000 1 2018 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
Liver and Intrahepatic Biliary Tract Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2018 2018
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.010 1.000 1 2018 2018
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 1.000 1 2018 2018
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 1.000 1 2018 2018
dbSNP: rs777906302
rs777906302
0.925 0.160 7 22728782 synonymous variant A/G;T snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.010 1.000 1 2018 2018