Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs978056
HECW1
1.000 0.120 7 43339245 intron variant G/A;T snv 1
rs9314614
GS1-24F4.2
1.000 0.120 8 6840209 intron variant C/G snv 0.61 2
rs9277535
HLA-DPB1
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs9138
SPP1
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs887280103
ACE
1.000 0.120 17 63477294 missense variant C/G snv 1.4E-05 1
rs859
STARD5 ; IL16
0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs8190315
BID
0.851 0.240 22 17743998 missense variant T/C snv 2.4E-02 3.6E-02 5
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs7790522
C1GALT1
1.000 0.120 7 7242918 intron variant A/G snv 0.30 1
rs7763262 1.000 0.120 6 32457105 downstream gene variant T/C snv 0.70 1
rs77370625
ZNF543
1.000 0.120 19 57328138 missense variant C/G snv 5.8E-03 2.8E-03 1
rs7634389
ST6GAL1
1.000 0.120 3 187020633 intron variant T/C snv 0.35 1
rs761991666
C1GALT1
1.000 0.120 7 7234516 missense variant A/G snv 4.0E-06 7.0E-06 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 4
rs7389
TREH ; PHLDB1
1.000 0.120 11 118657756 3 prime UTR variant T/G snv 0.32 1
rs719250
IL1R2
0.827 0.200 2 102007256 intron variant C/T snv 0.11 5
rs7190997
ITGAX
1.000 0.120 16 31356857 intron variant T/C snv 0.52 2
rs7170151
RASGRP1
1.000 0.120 15 38554477 intron variant C/T snv 0.40 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134