Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs777176672
PIK3R3 ; P3R3URF-PIK3R3
1.000 0.120 1 46066104 missense variant T/C snv 8.0E-06 1
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs4148323
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A4
0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 22
rs56161233
SH3BP4
0.925 0.120 2 235055489 3 prime UTR variant C/T snv 0.11 2
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs115160714
TOPBP1
0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs2230600
PTPN13
0.827 0.160 4 86769845 missense variant A/G snv 0.18 0.14 5
rs1864183
ATG10
0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs6877842
DROSHA ; C5orf22
0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs5744455
CD14 ; TMCO6
0.882 0.160 5 140633722 upstream gene variant G/A;T snv 5
rs28903090
RAD50
0.925 0.120 5 132587981 missense variant G/T snv 1.2E-03 1.4E-03 2
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs748148861
CCR6
0.925 0.120 6 167136856 missense variant G/C snv 8.0E-06 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4725443
KMT2C
0.925 0.120 7 152170176 intron variant T/C snv 9.3E-02 2