Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4
rs5758343 22 41420648 intergenic variant A/T snv 0.82 1
rs73205303
RUNX1
21 35095533 intron variant G/A snv 9.8E-02 1
rs76081789
SIK1
21 43426546 intron variant T/C snv 1
rs2766664
LOC101927770
1.000 0.080 20 53554702 intron variant A/G;T snv 2
rs3208007
RTEL1-TNFRSF6B ; RTEL1
1.000 0.080 20 63690935 synonymous variant T/C;G snv 0.74 2
rs3787184
NFATC2
1.000 0.120 20 51541298 intron variant A/G snv 0.17 2
rs6011033
RTEL1-TNFRSF6B ; RTEL1
20 63691346 intron variant A/G;T snv 2
rs6021268
NFATC2
20 51524602 intron variant T/C snv 5.8E-02 2
rs2766678
ZNF217
20 53591817 intron variant G/A snv 0.86 1
rs6021270
NFATC2
20 51524725 intron variant T/C snv 5.7E-02 1
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs4801001 18 54668944 intergenic variant T/C snv 0.62 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 4
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3
rs71368508
LOC105371498
1.000 0.040 17 4618178 downstream gene variant C/A snv 1.7E-02 3
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 2
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 2