Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs75002266
ORC4
0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs11715604
NCK1
0.851 0.160 3 136870707 intron variant A/G;T snv 4
rs1242982981
CLEC12A
0.851 0.160 12 9984989 missense variant C/T snv 4
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs131821
NCAPH2
0.851 0.160 22 50511648 intron variant T/-;TT;TTT;TTTT delins 4
rs149207840
SP140
0.851 0.160 2 230279864 intron variant CTGCCTC/-;CTGCCTCCTGCCTC delins 0.15 4
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4
rs1934951
CYP2C8
0.925 0.160 10 95038791 intron variant C/T snv 0.24 4
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 4
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs4273077
TNFRSF13B
0.925 0.160 17 16945825 intron variant A/G snv 0.13 4
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/A;C snv 4
rs6535455
HPSE
0.851 0.160 4 83310951 intron variant T/A;C snv 4
rs6546149
DTNB
0.851 0.160 2 25406569 intron variant C/G snv 0.38 4
rs6763508
ULK4
0.851 0.160 3 41709497 intron variant T/C snv 0.30 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs7372217
ULK4
1.000 0.160 3 41948630 intron variant G/A snv 0.68 4
rs7651190
ULK4
1.000 0.160 3 41724463 intron variant A/G snv 0.33 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4