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
rs11242417
GFRA3
1.000 0.040 5 138263645 intron variant T/G snv 0.13 2
rs11889798
C2orf83 ; LOC729968
1.000 0.120 2 227616703 intron variant C/T snv 0.13 2
rs12044963
KCND3
1.000 0.080 1 111849738 intron variant G/T snv 0.10 2
rs1403155 1.000 0.120 7 68585426 intergenic variant G/A snv 2.9E-02 2
rs1934953
CYP2C8
1.000 0.040 10 95037713 intron variant C/A;T snv 2
rs4713226
UBDP1
1.000 0.120 6 29466637 intron variant G/A;T snv 2
rs4963243
DAGLA
11 61726855 intron variant G/A snv 0.11 2
rs9807334 1.000 0.080 18 50997791 intron variant G/A snv 6.6E-02 2
rs10055544 5 92222904 intron variant G/A;T snv 1
rs10108684
ZHX2
8 122960828 intron variant G/A snv 0.11 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
rs10495471
GREM2
1 240542807 intron variant A/G snv 0.11 1
rs10503951
LOC105379364
8 33808162 intron variant A/G snv 6.2E-02 1
rs10508727
MKX
10 27736842 intron variant C/T snv 5.2E-02 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
rs10517025
ATP8A1
4 42451236 intron variant C/T snv 0.15 1
rs10998624
SUPV3L1
10 69180045 upstream gene variant G/A;T snv 1
rs11034653
LOC105376634
11 38267043 intergenic variant C/T snv 9.1E-02 1
rs11171846
TIMELESS
12 56434272 intron variant C/T snv 6.4E-02 1
rs11223581
CNTN5
11 100302805 intron variant A/G snv 5.6E-02 1
rs11564024 7 27295942 intergenic variant T/G snv 2.9E-02 1