Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9295924
LINC00243
0.925 0.120 6 30814584 non coding transcript exon variant G/A snv 0.27 0.17 5
rs9378109
LINC00243
0.925 0.120 6 30806697 intron variant C/A snv 0.16 5
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 4
rs204994
PBX2
0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 4
rs4937333
ETS1
0.882 0.120 11 128460625 3 prime UTR variant T/C snv 0.45 4
rs878329 0.882 0.120 17 5649930 intergenic variant G/C snv 0.44 4
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4
rs1049281
HLA-C
1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 3
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66 3
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs10919563
PTPRC
0.925 0.120 1 198731313 intron variant G/A snv 0.21 3
rs11466657
TLR10
0.925 0.120 4 38774173 missense variant A/G snv 2.7E-02; 4.0E-06 2.4E-02 3
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs150240657
AGBL2
0.925 0.120 11 47682026 missense variant G/A snv 8.7E-05 3.6E-04 3
rs17581834
IL19
0.882 0.120 1 206802774 intron variant T/C snv 4.2E-02 3
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs2277798
UBASH3A
0.925 0.120 21 42403997 missense variant A/G snv 0.55 0.60 3
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs2289263
SMAD3
0.925 0.120 15 67146869 intron variant T/G snv 0.43 3
rs2516399 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 3
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs2841277
PLD4
0.882 0.120 14 104924668 upstream gene variant C/T snv 0.41 3
rs2856437
PBX2
1.000 0.120 6 32189587 intron variant G/A snv 3.7E-02 3
rs2858310 1.000 0.120 6 32700546 TF binding site variant G/A snv 0.64 3