Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10886159 1.000 0.080 10 117854099 intergenic variant T/C snv 0.25 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs45565037
PHLDB1
1.000 0.080 11 118625403 intron variant G/A snv 0.20 1
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs11217040 0.925 0.200 11 118809939 regulatory region variant C/A snv 0.19 2
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs61579022
ARHGAP31
1.000 0.080 3 119404431 intron variant G/A snv 0.30 1
rs1997179 1.000 0.080 4 122063478 intergenic variant T/C snv 0.21 1
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 2
rs62323881 0.925 0.200 4 122117140 regulatory region variant C/A;T snv 2
rs11938795
KIAA1109
0.882 0.120 4 122151854 upstream gene variant T/C snv 0.24 3
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 7
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs11734090
KIAA1109
1.000 0.080 4 122306958 intron variant T/C snv 0.25 1
rs62321692
KIAA1109
1.000 0.080 4 122340375 intron variant A/C snv 5.1E-02 1
rs6851362
KIAA1109
1.000 0.080 4 122342291 intron variant T/C snv 0.25 1
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 3
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 10
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs531930
NKAIN2
1.000 0.080 6 124422361 intron variant A/G;T snv 1
rs4897233
THEMIS
1.000 0.080 6 127835743 intron variant A/G snv 0.38 1
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs10484718
THEMIS
1.000 0.080 6 127859906 intron variant A/T snv 8.6E-02 1