Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1700159
ACVRL1
1.000 0.040 12 51912002 intron variant C/A;G;T snv 4
rs1811069
YDJC
1.000 0.040 22 21627765 upstream gene variant T/A;G snv 4
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs71368508
LOC105371498
1.000 0.040 17 4618178 downstream gene variant C/A snv 1.7E-02 3
rs7713145 1.000 0.040 5 177354208 upstream gene variant G/A snv 0.37 3
rs10910095
LOC100996583
1.000 0.040 1 2579316 upstream gene variant G/A;C snv 2
rs10947428
ITPR3
1.000 0.040 6 33679281 intron variant T/C snv 0.26 2
rs11242709 1.000 0.040 6 209159 upstream gene variant C/T snv 0.19 2
rs11255753 1.000 0.040 10 8563590 intergenic variant G/C;T snv 0.23 2
rs11539209
ZDHHC12 ; PKN3
1.000 0.040 9 128721272 missense variant T/A;C snv 7.4E-02 2
rs2255088
PRKCQ-AS1
1.000 0.040 10 6583416 intron variant T/C snv 0.39 2
rs250308
LOC102723444 ; TNFAIP8
1.000 0.040 5 119348602 intron variant T/A;C snv 2
rs2744939 1.000 0.040 6 34580429 upstream gene variant T/A snv 0.17 2
rs4580194
GSDMA
1.000 0.040 17 39970224 intron variant A/G snv 0.41 2
rs519973 1.000 0.040 3 187915480 intergenic variant G/A snv 0.33 2
rs59185885
IL1RL1 ; IL18R1
1.000 0.040 2 102327786 intron variant T/G snv 0.18 2
rs60946162
LPP
1.000 0.040 3 188415548 intron variant C/T snv 0.35 2
rs61192126 1.000 0.040 3 72345701 intergenic variant T/C snv 0.26 2
rs6785012
ZBTB38
1.000 0.040 3 141390506 intron variant C/T snv 0.54 2
rs76167968 1.000 0.040 1 35216137 intergenic variant T/C snv 0.25 2
rs891058
LINC00299
1.000 0.040 2 8302417 non coding transcript exon variant G/A snv 0.23 2
rs10131567 1.000 0.040 14 35395672 intergenic variant G/T snv 0.22 1
rs10244416 1.000 0.040 7 20536128 intergenic variant C/A;T snv 0.52 1
rs1025549
PLCL1
1.000 0.040 2 198016459 intron variant G/A;T snv 1
rs1032841
LINC01814
1.000 0.040 2 8526108 intron variant A/G;T snv 1