Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs2074585
IQGAP1
0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67 5
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs1700159
ACVRL1
1.000 0.040 12 51912002 intron variant C/A;G;T snv 4
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 4
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 4
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 4
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs1811069
YDJC
1.000 0.040 22 21627765 upstream gene variant T/A;G snv 4
rs1870940
ZBTB7B
0.851 0.080 1 155011887 intron variant G/A snv 0.22 4
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs2390314 0.925 0.120 7 20416355 downstream gene variant A/C;T snv 3
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs7713145 1.000 0.040 5 177354208 upstream gene variant G/A snv 0.37 3
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs117137535
ARRDC1
0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 3
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs1214598
LOC101928512 ; CD247
0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv 3
rs115288876
LOC105371442
0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs71368508
LOC105371498
1.000 0.040 17 4618178 downstream gene variant C/A snv 1.7E-02 3