Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv 3
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs9611280
TNRC6B
1.000 0.120 22 40156115 missense variant G/A;T snv 6.8E-02; 5.1E-06 1
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs9378805 0.851 0.280 6 417727 intergenic variant A/C snv 0.36 4
rs9308731
BCL2L11 ; MIR4435-2HG
0.925 0.120 2 111150685 intron variant G/A snv 0.59 2
rs9288953
BTLA
1.000 0.120 3 112484405 intron variant C/T snv 0.27 1
rs9273363
HLA-DQB1-AS1
0.851 0.280 6 32658495 upstream gene variant C/A snv 0.23 4
rs9272535
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 7
rs9271176 0.925 0.120 6 32610350 intergenic variant A/G snv 0.69 2
rs9270750
HLA-DRB1
0.925 0.120 6 32600569 intergenic variant G/A snv 0.52 2
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 5
rs898518
LEF1
0.925 0.120 4 108095668 intron variant C/A;T snv 2
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs888096
LOC107985868
0.925 0.120 2 37376658 downstream gene variant G/A snv 0.55 2
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 8