Source: GWASDB

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: rs2736100
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0017638
Disease: Glioma
Glioma 		0.900 0.889 5 2009 2020
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.900 1.000 5 2008 2019
dbSNP: rs6010620
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0017638
Disease: Glioma
Glioma 		0.900 0.952 5 2009 2020
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 5 2007 2019
dbSNP: rs7756992
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 0.966 5 2007 2019
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 0.964 5 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 5 2009 2019
dbSNP: rs9277535
rs9277535
HLA-DPB1
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 5 2009 2018
dbSNP: rs1061170
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.900 0.936 4 2005 2019
dbSNP: rs11931074
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 1.000 4 2009 2020
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 4 2007 2019
dbSNP: rs2241880
rs2241880
ATG16L1 ; SCARNA5
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.900 0.961 4 2007 2020
dbSNP: rs3077
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.900 0.913 4 2009 2019
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 1.000 4 2008 2019
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0004096
Disease: Asthma
Asthma 		0.900 0.889 4 2007 2018
dbSNP: rs744373
rs744373 		0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.900 1.000 4 2011 2019
dbSNP: rs7901695
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 1.000 4 2006 2020
dbSNP: rs800292
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.900 0.980 4 2005 2019
dbSNP: rs10946398
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 1.000 3 2007 2019
dbSNP: rs11136000
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.900 0.913 3 2009 2018
dbSNP: rs11209026
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.900 0.773 3 2006 2020
dbSNP: rs11209026
rs11209026
IL23R
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: rs1990760
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.900 0.955 3 2007 2018
dbSNP: rs2104286
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.900 1.000 3 2007 2019
dbSNP: rs2200733
rs2200733 		0.752 0.240 4 110789013 intergenic variant C/T snv 0.18
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.900 0.971 3 2007 2019