Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11204971
FLG-AS1
0.925 0.120 1 152286602 intron variant A/G snv 0.15 2
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 2
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2
rs1528473 0.925 0.120 15 55094545 downstream gene variant A/G snv 7.6E-02 2
rs17718511
SPINK5
0.925 0.120 5 148072009 intron variant A/G snv 3.2E-02 2
rs2066446
IL12RB2
0.925 0.120 1 67315434 intron variant A/G snv 0.20 2
rs28441202
RPTN ; PUDPP2
0.925 0.120 1 152156387 missense variant A/G snv 2
rs3756094
IRF2
0.925 0.120 4 184429780 intron variant A/G snv 0.66 2
rs10067777
TMEM232
1.000 0.120 5 110490595 intron variant A/G snv 7.4E-02 1
rs1444418 1.000 0.120 10 62800710 intron variant A/G snv 0.22 1
rs16999165 1.000 0.120 20 54190682 intergenic variant A/G snv 5.5E-02 1
rs4674343
CYP27A1
1.000 0.120 2 218795623 intron variant A/G snv 0.48 1
rs7701890
TMEM232
1.000 0.120 5 110523120 intron variant A/G snv 0.15 1
rs7815944
LINC00824
1.000 0.120 8 128415272 intron variant A/G snv 0.12 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs438421
IL12RB1
0.882 0.200 19 18065276 intron variant A/G;T snv 3
rs9290927
LOC107986170
0.882 0.120 3 190304727 downstream gene variant A/G;T snv 3
rs11150780
SLC38A10
0.925 0.120 17 81290360 intron variant A/G;T snv 2
rs612529
VSTM1
0.925 0.120 19 54063999 upstream gene variant A/G;T snv 2
rs1665050
RNF111
1.000 0.120 15 59001406 intron variant A/G;T snv 1
rs2918307 1.000 0.120 19 8679458 downstream gene variant A/G;T snv 0.19 1
rs574456
LRP1B
0.882 0.160 2 140644133 intron variant A/T snv 8.1E-02 3
rs60978485
SPINK5
0.925 0.120 5 148091116 intron variant A/T snv 4.5E-02; 4.2E-06 3.2E-02 2
rs11205006 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 1