Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs10892286
DDX6
11 118771376 intron variant A/C snv 0.17 2
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs10932019 2 203764087 downstream gene variant G/A;C snv 2
rs10937560
MB21D2
0.882 3 192909627 intron variant G/C snv 0.45 4
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11043097
LINC02752
11 11114248 intron variant T/C snv 0.15 2
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11204735
ARNT
1.000 0.080 1 150869191 intron variant T/C snv 0.41 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1126407
LOC107985367 ; LGALS8
0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 5
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 5
rs1132200
TMEM39A
0.925 0.160 3 119431989 missense variant C/T snv 0.12 0.11 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490