Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10861905 0.925 0.120 12 108373556 regulatory region variant C/A snv 7.6E-02 1
rs10875943 0.925 0.080 12 49282227 intergenic variant T/A;C snv 1
rs10936632 0.925 0.080 3 170412314 intron variant C/A snv 0.41 1
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 1
rs11199874 0.925 0.080 10 121273005 intergenic variant G/A snv 0.23 1
rs11650494 0.925 0.080 17 49267824 intron variant G/A snv 0.12 1
rs12336160 0.925 0.120 9 33283584 downstream gene variant G/T snv 6.3E-02 1
rs1270884 0.925 0.080 12 114247766 intergenic variant A/G snv 0.63 1
rs1527243 0.925 0.120 2 122533446 intron variant C/G;T snv 1
rs17023900 0.925 0.080 3 87085650 upstream gene variant A/G snv 7.1E-02 1
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 1
rs4775302 0.925 0.080 15 46347610 intron variant G/A snv 0.49 1
rs7584330 0.925 0.080 2 237478585 intergenic variant A/G snv 0.38 1
rs7629490 0.925 0.080 3 87192347 intergenic variant C/T snv 0.32 1
rs7837688 0.925 0.080 8 127527115 intergenic variant T/G snv 0.91 1
rs7920517 0.925 0.080 10 46063201 upstream gene variant C/G;T snv 1
rs817826 0.925 0.080 9 107394019 intergenic variant C/T snv 0.81 1
rs902774 0.925 0.080 12 52880120 regulatory region variant G/A snv 0.12 1
rs9296068 0.925 0.200 6 33020918 intergenic variant T/G snv 0.42 1
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 1
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs1894292
AFM
0.925 0.080 4 73483441 intron variant G/A snv 0.42 1
rs6624304
AR
0.882 0.160 X 67655914 intron variant T/A;C snv 1