Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
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
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 1
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
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
rs7282490
GATD3A
0.882 0.080 21 44195858 intron variant G/A;T snv 4
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 3
rs2242944 1.000 0.040 21 39093252 intergenic variant G/A snv 0.46 1
rs378108 1.000 0.040 21 39097594 intergenic variant A/G snv 0.42 1
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
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