Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs76246107
PRR12
0.851 0.160 19 49618017 intron variant G/A snv 7.7E-02 4
rs7929541 0.851 0.160 11 633689 upstream gene variant T/C snv 0.34 4
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
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
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
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 4
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34