Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 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
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs10519067
RORA
0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
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
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 3
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3