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
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
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
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 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
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 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
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4