Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11586313 1 152917994 TF binding site variant G/A;C snv 0.51 2
rs6730714 2 222184302 intergenic variant G/A;T snv 2
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs3755967
GC
0.925 0.080 4 71743681 intron variant C/A;T snv 6
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv 4
rs17467825 0.925 0.080 4 71739800 downstream gene variant A/G snv 0.22 4
rs78862524
ADAMTS3
4 72305473 intron variant C/A snv 3.9E-02 3
rs13107347
NPFFR2
4 72109031 intron variant T/C snv 0.32 2
rs138485827 4 72166226 intergenic variant C/T snv 5.0E-02 2
rs148189294 4 71575200 downstream gene variant G/A snv 2.6E-02 2
rs1526692 4 71713007 intergenic variant A/G snv 0.41 2
rs1607741 4 71853316 intergenic variant G/C snv 0.65 2
rs17767445 4 71879550 intergenic variant G/A snv 0.20 2
rs79761689 4 72005565 intergenic variant T/C snv 3.7E-02 2
rs843005
GC
4 71750610 intron variant C/A;T snv 2
rs79666294 5 155047146 regulatory region variant C/T snv 2.2E-02 2
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs156299
LOC107986777
7 24185113 intergenic variant T/G snv 0.53 2
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8