Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs10024442
TMEM131L
1.000 0.080 4 153570903 intron variant T/G snv 0.13 1
rs10045595
TENM2
1.000 0.080 5 167802999 intron variant T/G snv 0.36 1
rs11030600 1.000 0.080 11 29174695 intron variant T/G snv 8.9E-02 1
rs11189017 1.000 0.080 10 81258621 intergenic variant T/G snv 1.0E-02 1
rs1652901 1.000 0.080 13 104748028 intergenic variant T/G snv 0.95 1
rs1857728 1.000 0.080 12 60331608 intergenic variant T/G snv 0.99 1
rs2523881 1.000 0.080 6 31074831 intergenic variant T/G snv 0.43 1
rs340397
LOC401324
1.000 0.080 7 35372753 non coding transcript exon variant T/G snv 0.59 1
rs3899582
MTUS2
0.882 0.120 13 29003859 intron variant T/G snv 1.9E-02 1
rs6059866
ITCH
1.000 0.080 20 34488005 intron variant T/G snv 0.45 1
rs6431360
LOC105373940
1.000 0.080 2 235272167 regulatory region variant T/G snv 0.77 1
rs9942466
SERAC1
1.000 0.080 6 158163377 intron variant T/G snv 2.7E-02 1
rs6670122
MRPL24
0.882 0.120 1 156737983 intron variant T/C;G snv 0.99 1
rs7694400 1.000 0.080 4 162571940 intergenic variant T/C;G snv 1
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs9268858
HLA-DRB9
0.882 0.200 6 32461981 intron variant T/C snv 0.29 5
rs4959093
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32345320 intron variant T/C snv 0.33 4
rs574710
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32320413 intron variant T/C snv 0.34 4
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 4
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 3
rs9267971 0.882 0.200 6 32249408 intergenic variant T/C snv 0.41 3
rs9268557 0.882 0.200 6 32421528 intergenic variant T/C snv 0.46 3