Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13298002 9 133279554 upstream gene variant G/A snv 5.9E-02 1
rs9411491 9 133280442 upstream gene variant T/C snv 0.18 2
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 4
rs1562064 4 145391948 intergenic variant G/A snv 0.74 2
rs2921604
ANKH
5 14867839 intron variant T/C snv 0.46 2
rs10265221
PRKAG2
7 151717243 intron variant T/A;C snv 3
rs12730935
IL6R
1 154447416 intron variant G/A snv 0.27 1
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 3
rs28491433
MSR1
8 16193362 intron variant C/G snv 0.19 1
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02 7
rs4273077
TNFRSF13B
0.925 0.160 17 16945825 intron variant A/G snv 0.13 4
rs4985726
TNFRSF13B
0.925 0.120 17 16960324 intron variant C/G snv 0.11 5
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs3733402
KLKB1
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54 5
rs2040771 22 19174422 downstream gene variant C/A;T snv 3
rs1998848
NDRG2 ; TPPP2 ; MIR6717
1.000 0.040 14 21024070 5 prime UTR variant G/A snv 1.6E-02 3
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs669408 1 232383404 regulatory region variant A/C snv 0.52 2
rs2006227
GGT1
22 24599789 intron variant C/A;T snv 2
rs115463265
RARB
3 24883579 intron variant C/T snv 2.4E-02 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20