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: rs2285714
rs2285714
PLA2G12A
0.882 0.040 4 109717654 synonymous variant C/T snv 0.37 0.31
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.810 0.500 1 2010 2019
dbSNP: rs2660753
rs2660753 		0.790 0.240 3 87061524 intergenic variant T/C snv 0.76
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.710 0.500 1 2008 2011
dbSNP: rs2823357
rs2823357
LOC105369302
1.000 0.040 21 15542586 intron variant G/A snv 0.48
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 0.500 1 2011 2019
dbSNP: rs3024490
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.710 0.500 1 2013 2017
dbSNP: rs34016896
rs34016896
LOC105374187
0.925 0.080 3 161275076 regulatory region variant C/T snv 0.28
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.710 0.500 1 2012 2015
dbSNP: rs3794087
rs3794087
SLC1A2
0.851 0.120 11 35308068 intron variant G/T snv 0.20
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.900 0.500 1 2012 2018
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.710 0.500 1 2011 2018
dbSNP: rs4730775
rs4730775
WNT2
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41
CUI: C4082974
Disease: Dupuytren's Disease
Dupuytren's Disease 		0.710 0.500 1 2011 2012
dbSNP: rs59336
rs59336
TBX3
0.776 0.160 12 114678547 intron variant T/A;G snv 0.49
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.810 0.500 1 2013 2014
dbSNP: rs6790925
rs6790925
LOC101927995 ; LOC105377013
0.925 0.040 3 30438593 intergenic variant C/G;T snv
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.810 0.500 1 2013 2014
dbSNP: rs7020673
rs7020673
GLIS3
0.882 0.200 9 4291747 intron variant C/A;G snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.810 0.500 1 2009 2017
dbSNP: rs7758229
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.810 0.500 1 2011 2013
dbSNP: rs7775228
rs7775228 		0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		0.810 0.500 1 2011 2020
dbSNP: rs9277534
rs9277534
HLA-DPB1
0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.710 0.500 1 2013 2018
dbSNP: rs9494266
rs9494266
LINC00271
1.000 0.080 6 135530435 intron variant G/A snv 0.27
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.710 0.500 1 2007 2008
dbSNP: rs995030
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67
CUI: C0855197
Disease: Malignant Testicular Germ Cell Tumor
Malignant Testicular Germ Cell Tumor 		0.710 0.500 1 2010 2016
dbSNP: rs1883025
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.740 0.600 1 2011 2018
dbSNP: rs3077
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.740 0.600 1 2011 2015
dbSNP: rs9818870
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.740 0.600 1 2011 2019
dbSNP: rs1893217
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.830 0.667 2 2009 2019
dbSNP: rs2458413
rs2458413
DPYS ; DCSTAMP
0.925 0.080 8 104347204 intron variant C/T snv 0.44
CUI: C0029401
Disease: Osteitis Deformans
Osteitis Deformans 		0.820 0.667 2 2010 2019
dbSNP: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.810 0.667 2 2009 2014
dbSNP: rs3135021
rs3135021
HLA-DPA1 ; HLA-DPB1
0.925 0.080 6 33077781 intron variant G/A snv 0.32
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.710 0.667 2 2009 2016
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		0.710 0.667 2 2010 2014
dbSNP: rs4309482
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.710 0.667 2 2011 2019