Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 4
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 4
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 4
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 3
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 3
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 3
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 3
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67 3
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 3
rs9273363
HLA-DQB1-AS1
0.851 0.280 6 32658495 upstream gene variant C/A snv 0.23 3
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 2
rs11668878
FKRP
0.925 0.200 19 46765116 intron variant G/T snv 5.1E-02 2
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 2
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 2
rs391525
IRF8
0.882 0.200 16 85910833 intron variant A/G;T snv 0.35 2
rs7169431 0.925 0.200 15 56048698 intergenic variant A/G;T snv 2
rs9378805 0.851 0.280 6 417727 intergenic variant A/C snv 0.36 2
rs1044873
IRF8
0.925 0.120 16 85922065 3 prime UTR variant C/T snv 0.40 1
rs11636802
LOC105370831
0.925 0.120 15 56483399 intergenic variant A/G snv 8.0E-02 1
rs11688943
PPIL3
1.000 0.120 2 200875545 intron variant T/C snv 0.30 1
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 1