Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 22
rs780094 0.699 0.286 2 27518370 intron variant T/C snp 0.67 20
rs1260326 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 20
rs579459 0.784 0.107 9 133278724 regulatory region variant C/T snp 0.20 17
rs653178 0.692 0.429 12 111569952 intron variant C/T snp 0.67 16
rs780093 0.923 0.071 2 27519736 intron variant T/C snp 0.68 16
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 16
rs9275572 0.685 0.321 6 32711222 intergenic variant A/G,T snp 0.57; 3.2E-05 15
rs657152 0.821 0.214 None NA snp 0.41 15
rs505922 0.724 0.357 None NA snp 0.37 13
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 13
rs886424 0.744 0.250 6 30814225 non coding transcript exon variant C/T snp 7.1E-02 9.1E-02 13
rs964184 0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83 13
rs651007 0.821 0.143 9 133278431 regulatory region variant T/A,C snp 0.20 12
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 12
rs4420638 0.724 0.321 19 44919689 intergenic variant A/G snp 0.19 12
rs204999 0.756 0.429 6 32142202 intergenic variant A/G snp 0.27 11
rs6932542 0.734 0.179 6 32412485 intergenic variant A/G snp 0.54 11
rs2647012 0.715 0.321 6 32696681 intergenic variant T/C snp 0.63 11
rs3764261 0.769 0.179 16 56959412 intergenic variant C/A snp 0.31 11
rs649129 0.923 0.107 9 133278860 regulatory region variant T/C,G snp 2.8E-02 11
rs687621 1.000 0.036 None NA snp 0.40 11
rs612169 1.000 0.036 None NA snp 0.40 11
rs2266788 0.846 0.286 11 116789970 3 prime UTR variant G/A snp 0.93 11
rs3763313 0.744 0.214 6 32408694 intergenic variant A/C snp 0.21 11