Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7533564
MGC27382 ; PTGFR
0.925 0.120 1 78360228 intron variant C/T snv 0.92 4
rs1233478
LINC02829
0.925 0.120 6 29510044 intron variant G/A;C;T snv 3
rs1264622
HLA-L ; HCG18 ; HCG17
1.000 0.120 6 30289159 non coding transcript exon variant C/T snv 0.13 3
rs13422767
FAP
0.882 0.120 2 162243749 intron variant G/A snv 0.14 3
rs17533090 1.000 0.120 6 32622945 TF binding site variant G/T snv 0.16 3
rs3130048
BAG6
1.000 0.120 6 31645962 intron variant T/C snv 0.23 3
rs3842727
TH
1.000 0.120 11 2163618 upstream gene variant G/T snv 0.58 3
rs428595
LOC107985532
1.000 0.120 22 21662102 non coding transcript exon variant A/G snv 0.98 3
rs6476839
GLIS3
0.925 0.120 9 4290823 intron variant A/C;T snv 3
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 3
rs754855896
HLA-DQB2
0.925 0.120 6 32758877 missense variant G/A;T snv 4.0E-06; 8.1E-06 3
rs927292
ZFP36L1
1.000 0.120 14 68792124 intron variant C/G snv 0.68 3
rs9273368
HLA-DQB1-AS1
0.882 0.120 6 32658698 upstream gene variant G/A snv 0.23 3
rs9273643
HLA-DQB1
0.925 0.120 6 32661407 missense variant A/G snv 3
rs1015166
TAP2
0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 2
rs10766196
CYP2R1
0.925 0.120 11 14891585 5 prime UTR variant A/G snv 0.35 2
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 2
rs10914542
LCK
0.925 0.120 1 32262639 intron variant C/G snv 0.15 2
rs1131568
TNFSF10
1.000 0.120 3 172505900 3 prime UTR variant T/C snv 0.70 2
rs11575248
STAT2
1.000 0.120 12 56342206 3 prime UTR variant G/T snv 4.5E-02 2
rs1223438908
CBLB
1.000 0.120 3 105681480 missense variant T/G snv 4.0E-06 2
rs13330041
CLEC16A
1.000 0.120 16 10994951 intron variant G/A snv 0.25 2
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 2
rs140101069
GLIS3
1.000 0.120 9 3828342 missense variant G/A snv 3.2E-04 8.4E-05 2
rs1419675 1.000 0.120 6 30124930 intergenic variant G/T snv 0.74 2