Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10683701
OS9
1.000 0.120 12 57698305 intron variant -/ACTT delins 0.61 1
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 2
rs3781094
GATA3
1.000 0.120 10 8059464 intron variant A/C snv 0.52 2
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs11121380
SPSB1
1.000 0.120 1 9348900 intron variant A/C snv 0.11 1
rs16906916
PCDH15
1.000 0.120 10 55089225 intron variant A/C snv 3.9E-02 1
rs2858884 0.925 0.200 6 32732306 upstream gene variant A/C snv 0.23 1
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 1
rs58999906 1.000 0.120 15 69862908 regulatory region variant A/C snv 6.1E-02 1
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 1
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 1
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 1
rs9269081
HLA-DRB9
0.851 0.280 6 32473323 intron variant A/C snv 0.69 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 3
rs2105325
TNFSF4 ; LOC100506023
1.000 0.120 1 173380586 intergenic variant A/C;G snv 1
rs9275428 0.925 0.120 6 32703201 downstream gene variant A/C;G snv 1
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs116199914
RARB
1.000 0.120 3 25596864 3 prime UTR variant A/C;G;T snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3