Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10067777
TMEM232
1.000 0.120 5 110490595 intron variant A/G snv 7.4E-02 1
rs10199605
LINC00299
1.000 0.120 2 8354967 intron variant G/A snv 0.26 1
rs10214237 1.000 0.120 5 35883632 downstream gene variant T/C snv 0.21 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10249788
LOC101927609 ; AHR
0.827 0.160 7 17298523 intron variant C/G;T snv 6
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs1057518775
KCNJ11
0.851 0.160 11 17387907 missense variant G/A;C snv 4
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs10738626 1.000 0.120 9 22373458 intergenic variant C/G;T snv 1
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs10888499 1.000 0.120 1 152560266 intergenic variant C/A;T snv 1
rs10995251
LOC105378327 ; ZNF365
1.000 0.120 10 62638706 intron variant C/T snv 0.29 1
rs11079788
TBX21
0.925 0.120 17 47743357 intron variant C/T snv 0.23 2
rs11150780
SLC38A10
0.925 0.120 17 81290360 intron variant A/G;T snv 2
rs11167761
PCDH1
0.925 0.120 5 141858778 intron variant G/A snv 0.14 2
rs11204971
FLG-AS1
0.925 0.120 1 152286602 intron variant A/G snv 0.15 2
rs11205006 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 1
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 2
rs113136594
FLG ; FLG-AS1
0.925 0.120 1 152313436 missense variant G/A;C;T snv 6.0E-04; 4.0E-06; 8.0E-06 2
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs11558538
LOC107985948 ; HNMT
0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs115746363
FLG-AS1 ; FLG
0.882 0.120 1 152312410 stop gained G/A;C snv 6.0E-04 3
rs11584340
FLG ; FLG-AS1
0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2