Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150768229
FGB
4 154567149 intron variant A/C snv 9.5E-03 1
rs1539019
NLRP3
0.882 0.240 1 247436999 intron variant A/C snv 0.63 1
rs1938492 1 65652146 intergenic variant A/C snv 0.43 1
rs6010044 22 50663510 intergenic variant A/C snv 0.20 1
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 2
rs7004769
LOC157273
8 9330085 intron variant A/C;G snv 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
rs8026198
CAPN3
15 42361263 intron variant A/C;T snv 1
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 5
rs7935829
MS4A6A
1.000 0.080 11 60175342 intron variant A/G snv 0.33 3
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs12528797
TSBP1-AS1
6 32377309 intron variant A/G snv 1.0E-01 1
rs12598049
CHD9
16 53282942 intron variant A/G snv 0.28 1
rs12712127
IL1R1
2 102110201 intron variant A/G snv 0.62 1
rs12915052
SPPL2A
15 50732090 intron variant A/G snv 0.24 1
rs194741 14 68821715 intergenic variant A/G snv 0.24 1
rs2376015 1 65658091 intergenic variant A/G snv 0.43 1
rs367677 14 68806373 intergenic variant A/G snv 0.25 1
rs7968440
DIP2B
12 50740958 intron variant A/G snv 0.28 1
rs35489971
CD300LF ; RAB37
1.000 0.040 17 74704804 missense variant A/G;T snv 0.73 2
rs11242111
LINC02863 ; IRF1-AS1
5 132420366 intron variant A/G;T snv 1
rs1476698
FARP2
2 241357034 intron variant A/G;T snv 1
rs511154 3 136232079 intergenic variant A/G;T snv 1
rs7916868
JMJD1C
10 63229171 intron variant A/T snv 0.47 3