Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 4
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 3
rs183211
LRRC37A2 ; NSF
0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 3
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 2
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 2
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 2
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 2
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 2
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 2
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 2
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 1
rs142091544 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 1
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs1614627 1.000 0.120 1 20620263 downstream gene variant A/C snv 0.86 1
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 1
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 1
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 1
rs7230264 1.000 0.120 18 27347470 intron variant G/A snv 0.15 1
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 1