Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 4
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 1
rs10893845 11 128316987 regulatory region variant T/G snv 0.36 1
rs2197415 10 9020893 intergenic variant T/G snv 0.66 1
rs6461503 0.925 0.080 7 20521373 intergenic variant T/C;G snv 3
rs3208007
RTEL1-TNFRSF6B ; RTEL1
1.000 0.080 20 63690935 synonymous variant T/C;G snv 0.74 2
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 4
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs10008032
LOC105374413
1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 2
rs10947428
ITPR3
1.000 0.040 6 33679281 intron variant T/C snv 0.26 2
rs1612986 0.925 0.080 10 9022753 intergenic variant T/C snv 0.24 2
rs45605540
KIAA1109
1.000 0.080 4 122219899 intron variant T/C snv 0.20 2
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 2
rs6021268
NFATC2
20 51524602 intron variant T/C snv 5.8E-02 2
rs61192126 1.000 0.040 3 72345701 intergenic variant T/C snv 0.26 2