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: rs992969
rs992969
2 0.882 0.080 9 6209697 intergenic variant A/G;T snv 0.810 1.000 1 2010 2019
dbSNP: rs9916158
rs9916158
1 1.000 0.080 17 40025976 intron variant G/T snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs9909593
rs9909593
3 0.925 0.160 17 39813896 intron variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9907088
rs9907088
3 0.925 0.160 17 39878863 downstream gene variant G/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs9904624
rs9904624
2 0.925 0.160 17 39880333 downstream gene variant A/G snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs9901146
rs9901146
3 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 0.800 1.000 1 2011 2019
dbSNP: rs9891949
rs9891949
1 1.000 0.080 17 8195865 downstream gene variant G/A snv 0.64 0.700 1.000 1 2012 2012
dbSNP: rs987870
rs987870
3 0.851 0.160 6 33075103 intron variant A/G snv 0.19 0.810 1.000 1 2011 2011
dbSNP: rs983280
rs983280
1 1.000 0.080 5 60149310 intron variant C/T snv 0.68 0.700 1.000 2 2009 2010
dbSNP: rs9807989
rs9807989
1 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 0.800 1.000 1 2012 2012
dbSNP: rs9792269
rs9792269
5 0.882 0.200 8 128252343 intergenic variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs9570077
rs9570077
1 1.000 0.080 13 59245009 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs9500927
rs9500927
1 1.000 0.080 6 32993584 regulatory region variant G/A snv 0.19 0.800 1.000 1 2011 2011
dbSNP: rs949963
rs949963
2 0.925 0.160 2 102153326 intron variant C/T snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs946263
rs946263
1 1.000 0.080 1 203196253 intergenic variant G/A snv 0.86 0.700 1.000 1 2000 2000
dbSNP: rs931992
rs931992
1 1.000 0.080 17 39665182 upstream gene variant G/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs9303281
rs9303281
4 0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs9303280
rs9303280
2 1.000 0.080 17 39917778 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs9303277
rs9303277
4 0.790 0.240 17 39820216 intron variant C/T snv 0.52 0.720 1.000 2 2010 2017
dbSNP: rs9286879
rs9286879
4 0.851 0.200 1 172893094 intron variant A/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs928413
rs928413
2 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 0.800 1.000 1 2010 2019
dbSNP: rs9275698
rs9275698
2 0.925 0.160 6 32720196 downstream gene variant A/G snv 0.37 0.800 1.000 1 2011 2011
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: rs9272346
rs9272346
6 0.790 0.320 6 32636595 intron variant G/A snv 0.54 0.810 1.000 1 2012 2019
dbSNP: rs9268853
rs9268853
8 0.790 0.440 6 32461866 intron variant T/C snv 0.29 0.700 1.000 1 2012 2012