Source: GWASCAT

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: rs6920220
rs6920220
0.742 0.440 6 137685367 intron variant G/A snv 0.16
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.900 0.938 6 2007 2019
dbSNP: rs7756992
rs7756992
0.827 0.240 6 20679478 intron variant A/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.966 6 2007 2019
dbSNP: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 5 2007 2020
dbSNP: rs1470579
rs1470579
0.925 0.160 3 185811292 intron variant A/C snv 0.46
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.963 5 2007 2017
dbSNP: rs2046210
rs2046210
0.708 0.280 6 151627231 intergenic variant G/A snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.900 1.000 5 2009 2019
dbSNP: rs2106261
rs2106261
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.900 0.929 5 2009 2019
dbSNP: rs6656401
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 1.000 5 2009 2019
dbSNP: rs7754840
rs7754840
0.807 0.200 6 20661019 intron variant G/A;C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.958 5 2007 2019
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.900 0.964 4 2008 2019
dbSNP: rs10795668
rs10795668
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 1.000 4 2008 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.900 1.000 4 2004 2019
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.902 4 1997 2018
dbSNP: rs2230926
rs2230926
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.900 0.867 4 2008 2019
dbSNP: rs5219
rs5219
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.906 4 1998 2019
dbSNP: rs738409
rs738409
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.900 0.953 4 2009 2020
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.964 4 2007 2019
dbSNP: rs8099917
rs8099917
0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.900 1.000 4 2009 2019
dbSNP: rs9277535
rs9277535
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.900 0.917 4 2009 2018
dbSNP: rs1006737
rs1006737
0.695 0.120 12 2236129 intron variant G/A snv 0.36
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.900 1.000 3 2010 2019
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.900 1.000 3 2008 2018
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.900 1.000 3 2007 2020
dbSNP: rs1143679
rs1143679
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.900 1.000 3 2009 2019
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0028754
Disease: Obesity
Obesity
0.900 1.000 3 2007 2019
dbSNP: rs1990760
rs1990760
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45
Diabetes Mellitus, Insulin-Dependent
0.900 0.955 3 2007 2018
dbSNP: rs3865444
rs3865444
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 1.000 3 2011 2019