Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs993226
LOC105369875
0.851 0.160 12 84492794 intergenic variant T/G snv 6.3E-02 4
rs976078 0.882 0.120 13 82963398 intron variant A/C snv 0.15 4
rs9469099
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32341131 intron variant G/A;T snv 1
rs941934
FLG-AS1
0.851 0.200 1 152417976 intron variant T/A;C snv 5
rs941505
TGM1
0.925 0.120 14 24264066 5 prime UTR variant T/A;C snv 2
rs9405490
LOC102723944
0.925 0.120 6 1510423 downstream gene variant G/A snv 0.20 2
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 8
rs9368677
LOC112267902 ; HLA-B
1.000 0.120 6 31304544 intron variant G/A snv 7.4E-02 1
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs9302874 0.925 0.120 17 78284479 intergenic variant C/T snv 0.24 2
rs9290929
CLDN16
0.925 0.120 3 190325950 intron variant G/A snv 0.65 2
rs9290927
LOC107986170
0.882 0.120 3 190304727 downstream gene variant A/G;T snv 3
rs909341
RTEL1-TNFRSF6B ; TNFRSF6B
1.000 0.120 20 63697389 synonymous variant C/T snv 0.25 0.19 1
rs9050
TCHH
1.000 0.120 1 152106838 3 prime UTR variant C/A snv 4.3E-02 1
rs895691
NAT9
0.925 0.120 17 74770161 downstream gene variant C/A;T snv 2
rs893051
CLDN1
0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs878906
NAT9
0.925 0.120 17 74773195 non coding transcript exon variant T/C snv 0.51 2
rs878860 0.882 0.120 11 7946812 intergenic variant C/T snv 0.35 3
rs877776
LOC112268240 ; FLG-AS1
0.925 0.120 1 152205542 intron variant C/G;T snv 2
rs80312298
MGMT
0.925 0.120 10 129683009 intron variant C/A;T snv 2
rs795467
IL18
0.925 0.120 11 112160357 intron variant G/A;C;T snv 2
rs793814
IRF2
0.925 0.120 4 184433820 intron variant T/A snv 0.70 2
rs7936562 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 4
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12