Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9807334 1.000 0.080 18 50997791 intron variant G/A snv 6.6E-02 2
rs12044963
KCND3
1.000 0.080 1 111849738 intron variant G/T snv 0.10 2
rs2834655
RUNX1
21 34866210 intron variant G/A snv 0.28 2
rs10055544 5 92222904 intron variant G/A;T snv 1
rs10195263 2 150869278 intergenic variant G/A;C snv 1
rs10432496 2 149290764 regulatory region variant C/A;T snv 1
rs10513432 3 152817576 regulatory region variant T/C snv 0.12 1
rs11564024 7 27295942 intergenic variant T/G snv 2.9E-02 1
rs12247397 10 9321914 intergenic variant A/G snv 2.2E-02 1
rs13111850 4 167343098 intergenic variant C/T snv 0.97 1
rs1372791 13 106132916 regulatory region variant T/C snv 0.94 1
rs1392089 6 119544976 intergenic variant C/T snv 6.8E-02 1
rs1403155 1.000 0.120 7 68585426 intergenic variant G/A snv 2.9E-02 1
rs1473500 6 168110336 intergenic variant C/T snv 0.19 1
rs16948200 17 49488950 intergenic variant G/A;C snv 1
rs17007761 2 122468047 intron variant C/A snv 6.0E-02 1
rs17142462 7 119966578 intergenic variant C/A;T snv 1
rs17331151 3 52810518 downstream gene variant C/T snv 7.5E-02 1
rs2043599 19 55939683 intergenic variant A/G snv 5.9E-02 1
rs381365 X 146667390 intergenic variant T/G snv 1
rs4827947 X 98609356 intron variant T/A;C snv 1
rs6576443 15 25649511 intergenic variant C/T snv 0.42 1
rs738968 22 34493105 intergenic variant T/G snv 0.11 1
rs859267 17 15922707 intergenic variant A/C;G snv 1
rs17231212
AGBL3 ; CYREN
7 135100989 intron variant T/C snv 6.1E-02 1