Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 6
rs140135
ZMAT5 ; UQCR10
0.827 0.120 22 29767846 non coding transcript exon variant C/G snv 0.79 5
rs5757584 0.827 0.120 22 39266545 intron variant C/G;T snv 5
rs145832854
SGSM1
1.000 0.040 22 24914162 intron variant G/A snv 3.1E-02 1
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 6
rs2823288 0.827 0.120 21 15448569 intron variant G/A snv 0.22 5
rs4456788
GATD3A
0.827 0.120 21 44196441 intron variant G/A snv 5
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 3
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs6058869
DNMT3B
0.827 0.120 20 32760944 upstream gene variant C/T snv 0.55 6
rs6062496
TNFRSF6B ; RTEL1-TNFRSF6B
0.827 0.120 20 63697746 intron variant G/A snv 0.52 6
rs1328454
SLC9A8
0.827 0.120 20 49823486 intron variant T/C snv 0.57 5
rs4812833
LINC01620
0.827 0.120 20 44440356 intron variant G/A;C snv 5
rs79493594
PKIG
0.827 0.120 20 44561731 intron variant C/T snv 2.1E-02 5
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs35074907
KEAP1
0.807 0.160 19 10489742 synonymous variant G/A snv 1.9E-02 1.5E-02 6
rs4802307
PPP5C
0.827 0.120 19 46346549 upstream gene variant G/T snv 0.21 6