Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25 2
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36 2
rs12948909
CAVIN1
0.925 0.120 17 42418584 intron variant A/C snv 0.24 1
rs16853571
PHOX2B-AS1
1.000 0.040 4 41751113 intron variant A/C snv 9.9E-02 1
rs16931910
DELEC1
1.000 0.040 9 114856029 intron variant A/C snv 7.2E-02 1
rs17312836
NOD2
1.000 0.040 16 50707551 intron variant A/C snv 0.33 1
rs2382817
PNKD ; TMBIM1
0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 1
rs247660 1.000 0.040 5 85462322 upstream gene variant A/C snv 0.21 1
rs3135499
NOD2
0.882 0.160 16 50732216 splice donor variant A/C snv 0.45 1
rs4855873
AMT
1.000 0.040 3 49421681 non coding transcript exon variant A/C snv 0.43 1
rs7186163 1.000 0.040 16 50652646 downstream gene variant A/C snv 0.63 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs10512734 1.000 0.040 5 40393503 intergenic variant A/C;G snv 0.29 1
rs11871801
CAVIN1
1.000 0.040 17 42418754 intron variant A/C;G snv 1
rs2302759
LOC105371251 ; CYLD
1.000 0.040 16 50793690 intron variant A/C;G snv 4.0E-06; 0.79 1
rs394522 1.000 0.040 6 166984583 intron variant A/C;G snv 1
rs7076156
ZNF365 ; LOC105378327
0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 1
rs740495
SBNO2
1.000 0.040 19 1124836 intron variant A/C;G snv 1