Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2834655
RUNX1
21 34866210 intron variant G/A snv 0.28 3
rs1403155 1.000 0.120 7 68585426 intergenic variant G/A snv 2.9E-02 2
rs9807334 1.000 0.080 18 50997791 intron variant G/A snv 6.6E-02 2
rs11889798
C2orf83 ; LOC729968
1.000 0.120 2 227616703 intron variant C/T snv 0.13 2
rs1934953
CYP2C8
1.000 0.040 10 95037713 intron variant C/A;T snv 2
rs4963243
DAGLA
11 61726855 intron variant G/A snv 0.11 2
rs11242417
GFRA3
1.000 0.040 5 138263645 intron variant T/G snv 0.13 2
rs12044963
KCND3
1.000 0.080 1 111849738 intron variant G/T snv 0.10 2
rs4713226
UBDP1
1.000 0.120 6 29466637 intron variant G/A;T snv 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
rs10489759 1 189620209 regulatory region variant C/T snv 0.17 1
rs10512697 5 3558424 intergenic variant T/C snv 5.3E-02 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
rs12256830 10 53624983 intergenic variant C/T snv 5.5E-02 1
rs12775535 10 25629950 intergenic variant C/T snv 2.9E-02 1
rs13111850 4 167343098 intergenic variant C/T snv 0.97 1
rs1322846 6 17240923 intron variant T/C snv 0.39 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
rs1473500 6 168110336 intergenic variant C/T snv 0.19 1
rs16948200 17 49488950 intergenic variant G/A;C snv 1