Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4958880
TNIP1
0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs11085725
TYK2
0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs114042950 1.000 0.080 6 32699098 intergenic variant A/G snv 1
rs114388793 1.000 0.080 6 32699566 intergenic variant A/T snv 1
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 1
rs114050967
DDX39B ; ATP6V1G2-DDX39B ; SNORD117
1.000 0.080 6 31537703 intron variant A/G snv 1
rs9267488
DDX39B ; NFKBIL1 ; ATP6V1G2-DDX39B ; ATP6V1G2
1.000 0.080 6 31546470 splice region variant A/G snv 8.1E-02 9.9E-02 1
rs6599390
DGKQ
1.000 0.080 4 962259 intron variant A/G snv 0.69 1
rs114012716
HCP5
1.000 0.080 6 31466589 non coding transcript exon variant G/A snv 1
rs115146037
HCP5
1.000 0.080 6 31466554 non coding transcript exon variant A/T snv 1
rs115902351
HCP5
1.000 0.080 6 31466844 non coding transcript exon variant A/G snv 1
rs116088953
HCP5
1.000 0.080 6 31475005 intron variant G/A snv 1
rs3130614
MICB
1.000 0.080 6 31508681 intron variant T/A snv 7.3E-02 1
rs114771815
MICB-DT
1.000 0.080 6 31484059 intron variant T/C snv 1
rs116662199
MICB-DT
1.000 0.080 6 31481199 non coding transcript exon variant C/A snv 1