Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs464138
MX1
1.000 0.080 21 41426246 5 prime UTR variant A/C snv 0.36 1
rs522127
LINC01100 ; IL12A-AS1
1.000 0.080 3 160016881 intron variant A/C snv 0.41 1
rs6677309
CD58
1.000 0.080 1 116537544 intron variant A/C snv 0.28 1
rs669607
LINC01967
1.000 0.080 3 28029953 intron variant A/C snv 0.38 1
rs759648
PVT1
1.000 0.080 8 128146699 intron variant A/C snv 0.33 1
rs104895271
TNFRSF1A
0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs3957148 0.925 0.160 6 32714360 upstream gene variant A/C;G snv 0.10 4
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 3
rs1801406
BRCA2
1.000 0.080 13 32337751 missense variant A/C;G snv 0.29 2
rs1920296
IQCB1
1.000 0.080 3 121824730 intron variant A/C;G snv 2
rs4285028
SLC15A2
1.000 0.080 3 121941817 3 prime UTR variant A/C;G snv 2
rs148561683
PTPRC
1.000 0.080 1 198703360 missense variant A/C;G snv 5.3E-04; 1.2E-05 1
rs175126
LOC105369325
1.000 0.080 11 61066152 intron variant A/C;G snv 1
rs1805755
KLRG1 ; M6PR
1.000 0.080 12 8949816 upstream gene variant A/C;G snv 1.7E-02 1
rs2080272
CLEC16A
1.000 0.080 16 11117696 intron variant A/C;G snv 1
rs6896969 1.000 0.080 5 40424324 intron variant A/C;G snv 0.57 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs3134603
PPT2-EGFL8 ; PPT2
0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs2905747
MICB-DT
1.000 0.080 6 31483699 intron variant A/C;G;T snv 1
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67