Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1050283
OLR1
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4
rs1774093 1.000 0.080 9 101884874 intergenic variant A/G snv 0.12 1
rs115641191 1.000 0.080 4 102133052 intergenic variant C/T snv 6.2E-03 1
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs2852894 1.000 0.080 11 102284743 intergenic variant A/G snv 0.93 1
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 4
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs363043
SNAP25-AS1 ; SNAP25
0.925 0.080 20 10245498 intron variant C/T snv 0.30 3
rs748799635
IGF1
1.000 0.080 12 102475727 missense variant C/T snv 8.0E-06 1
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs223493
MANBA
1.000 0.080 4 102747187 intron variant T/G snv 0.29 1
rs3025079
MMP3 ; WTAPP1
1.000 0.080 11 102835973 3 prime UTR variant C/T snv 2.0E-02 1
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 5
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs520540
MMP3
0.925 0.120 11 102838694 synonymous variant A/G snv 0.57 0.54 2
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs573521 1.000 0.080 11 102846249 upstream gene variant A/G snv 0.57 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs12808148
MMP12
1.000 0.080 11 102862432 downstream gene variant T/C snv 0.12 1
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs223330
CISD2
0.851 0.160 4 102872502 intron variant T/A;C snv 4
rs6468852
AZIN1-AS1
1.000 0.080 8 102963761 intron variant A/G snv 0.30 1
rs76070545 1.000 0.080 8 103359219 intergenic variant T/C snv 3.6E-02 1