Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 19
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17