Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 1
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 1
rs10260419
THSD7A
0.882 0.120 7 11524758 intron variant C/G snv 0.26 1
rs17329882
SYNPO2
0.925 0.120 4 119028805 intron variant A/C;T snv 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 2
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 1
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 2
rs9283636 1.000 0.120 3 166315136 intergenic variant G/A snv 0.46 1
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs142091544 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 1
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 2
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 2
rs1614627 1.000 0.120 1 20620263 downstream gene variant A/C snv 0.86 1
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 2
rs3820282
LOC105376845 ; WNT4
0.925 0.120 1 22141722 intron variant C/T snv 0.13 1
rs56318008
LOC105376845 ; WNT4
0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13 1
rs74917072
UBE2F ; UBE2F-SCLY
0.882 0.120 2 238022053 intron variant G/A;T snv 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs7230264 1.000 0.120 18 27347470 intron variant G/A snv 0.15 1
rs115344852
GPX6
1.000 0.120 6 28518321 intron variant A/C snv 1
rs2070074
GALT
0.742 0.360 9 34649445 missense variant A/G snv 9.2E-02 7.4E-02 1