Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 5
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
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs3129843 0.827 0.160 6 32427949 intergenic variant A/G snv 6.3E-02 4
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs7929541 0.851 0.160 11 633689 upstream gene variant T/C snv 0.34 4
rs1217393
AP4B1-AS1
0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs5754467
CCDC116 ; YDJC
0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs10954214
IRF5
0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs2422345
LOC100506023 ; TNFSF4
0.851 0.160 1 173368608 upstream gene variant G/A snv 0.63 4
rs76246107
PRR12
0.851 0.160 19 49618017 intron variant G/A snv 7.7E-02 4
rs13389408
STAT4
0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4