Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10954214
IRF5
0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs11085725
TYK2
0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs114012716
HCP5
1.000 0.080 6 31466589 non coding transcript exon variant G/A snv 1
rs114042950 1.000 0.080 6 32699098 intergenic variant A/G snv 1
rs114050967
DDX39B ; ATP6V1G2-DDX39B ; SNORD117
1.000 0.080 6 31537703 intron variant A/G snv 1
rs114388793 1.000 0.080 6 32699566 intergenic variant A/T snv 1
rs114771815
MICB-DT
1.000 0.080 6 31484059 intron variant T/C 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
rs116662199
MICB-DT
1.000 0.080 6 31481199 non coding transcript exon variant C/A snv 1
rs1217393
AP4B1-AS1
0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs13389408
STAT4
0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4
rs17849502
NCF2 ; SMG7
0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 1
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs2422345
LOC100506023 ; TNFSF4
0.851 0.160 1 173368608 upstream gene variant G/A snv 0.63 4
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 4