Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 4
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs115288876
LOC105371442
0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs1214598
LOC101928512 ; CD247
0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv 3
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs10910095
LOC100996583
1.000 0.040 1 2579316 upstream gene variant G/A;C snv 2
rs12743520
EVI5
1.000 0.080 1 92571555 intron variant C/A snv 0.20 2
rs2070902
FCER1G
1.000 0.120 1 161217875 intron variant C/T snv 0.31 2
rs61815704 1.000 0.080 1 152921415 intergenic variant C/G snv 1.1E-02 2
rs61816766
FLG-AS1
1.000 0.080 1 152347096 intron variant T/C snv 1.6E-02 2
rs742230
RUNX3 ; LOC107984932
1.000 0.080 1 24924933 intron variant G/A snv 0.53 2
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 2
rs76167968 1.000 0.040 1 35216137 intergenic variant T/C snv 0.25 2
rs11204896
RORC
1 151824266 intron variant C/G snv 7.6E-02 1
rs12045923
PEX14
1 10583772 intron variant C/G;T snv 1
rs2056417
PEX14
1 10521601 intron variant G/A snv 0.25 1
rs2988277
CD247
1 167462115 intron variant C/T snv 0.27 1
rs4090390 1 173177782 upstream gene variant C/A snv 0.29 1
rs4908769
RERE
1 8641229 intron variant C/T snv 0.27 1