Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 4
rs131821
NCAPH2
0.851 0.160 22 50511648 intron variant T/-;TT;TTT;TTTT delins 4
rs1439112
MGAT5
0.851 0.160 2 134305027 intron variant G/A snv 0.61 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
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
rs2777899
VMP1
0.851 0.160 17 59755030 intron variant T/A;G snv 4
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 4
rs35603048
BMF
0.851 0.160 15 40099764 intron variant C/A;G;T snv 4
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/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
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs757978
FARP2
0.851 0.200 2 241431686 missense variant C/A;T snv 4.1E-06; 9.3E-02 4
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs9273363
HLA-DQB1-AS1
0.851 0.280 6 32658495 upstream gene variant C/A snv 0.23 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45 3
rs11083846
PRKD2
0.882 0.200 19 46704397 splice region variant G/A snv 0.17 0.16 3
rs1292034
RPS6KB1
0.882 0.160 17 59912499 intron variant G/A snv 0.56 3