Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7216389
rs7216389
3 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.900 0.889 4 2007 2018
dbSNP: rs2305480
rs2305480
7 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 0.860 0.900 4 2008 2018
dbSNP: rs1295686
rs1295686
2 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 0.840 1.000 3 2010 2018
dbSNP: rs1342326
rs1342326
2 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 0.840 1.000 3 2010 2020
dbSNP: rs1837253
rs1837253
2 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 0.840 0.929 3 2010 2019
dbSNP: rs11071559
rs11071559
1 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.820 1.000 3 2010 2019
dbSNP: rs11078927
rs11078927
2 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 0.820 1.000 2 2011 2018
dbSNP: rs2290400
rs2290400
6 0.790 0.360 17 39909987 intron variant T/C snv 0.48 0.820 1.000 2 2010 2016
dbSNP: rs2244012
rs2244012
1 1.000 0.080 5 132565533 intron variant A/G snv 0.33 0.820 1.000 1 2010 2016
dbSNP: rs3771180
rs3771180
2 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 0.820 1.000 1 2011 2019
dbSNP: rs3859192
rs3859192
3 0.925 0.080 17 39972395 intron variant C/T snv 0.42 0.820 1.000 1 2010 2016
dbSNP: rs4129267
rs4129267
5 0.807 0.200 1 154453788 intron variant C/G;T snv 0.820 0.667 1 2011 2018
dbSNP: rs7212938
rs7212938
1 0.925 0.120 17 39966427 missense variant G/A;C;T snv 4.1E-04; 4.2E-06; 0.52 0.820 0.750 1 2011 2015
dbSNP: rs7927894
rs7927894
5 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 0.820 0.750 1 2011 2018
dbSNP: rs3894194
rs3894194
2 0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 0.810 1.000 4 2010 2014
dbSNP: rs2284033
rs2284033
2 0.790 0.160 22 37137994 intron variant G/A snv 0.43 0.810 1.000 3 2010 2012
dbSNP: rs3771166
rs3771166
2 1.000 0.080 2 102369762 intron variant G/A;T snv 0.810 1.000 3 2010 2012
dbSNP: rs744910
rs744910
1 1.000 0.080 15 67154447 intron variant G/A;T snv 0.810 1.000 3 2010 2012
dbSNP: rs907092
rs907092
3 0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 0.810 1.000 3 2010 2019
dbSNP: rs9273349
rs9273349
1 0.827 0.200 6 32658092 upstream gene variant T/C;G snv 0.810 1.000 3 2010 2012
dbSNP: rs13408661
rs13408661
2 1.000 0.080 2 102338622 intron variant G/A snv 0.18 0.810 1.000 2 2011 2012
dbSNP: rs4794820
rs4794820
3 0.790 0.160 17 39933091 intron variant A/G;T snv 0.810 1.000 2 2011 2012
dbSNP: rs6503525
rs6503525
2 0.925 0.080 17 39938921 intron variant G/A;C snv 0.810 1.000 2 2011 2015
dbSNP: rs10197862
rs10197862
2 0.925 0.120 2 102350089 intron variant A/G snv 0.18 0.810 1.000 1 2011 2014
dbSNP: rs2786098
rs2786098
1 1.000 0.080 1 197356778 intron variant T/A;G snv 0.810 1.000 1 2010 2010