Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs189897
ITGA9
1.000 0.120 3 37477054 intron variant T/A snv 0.13 1
rs197757
ITGA9
1.000 0.120 3 37481337 intron variant G/A snv 0.14 1
rs2212020
ITGA9
1.000 0.120 3 37475971 intron variant C/T snv 0.34 1
rs6774494
MECOM
0.882 0.160 3 169364845 intron variant G/A snv 0.42 1
rs8049883
MT1A
1.000 0.120 16 56639498 intron variant G/A snv 0.15 1
rs10163267
OSGIN1 ; MLYCD ; LOC105371371
1.000 0.120 16 83940313 intron variant G/A;C snv 1
rs2305806
SH2D3A
1.000 0.120 19 6754996 synonymous variant T/C snv 0.30 0.35 1
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 1
rs9510787
TNFRSF19
1.000 0.120 13 23631056 intron variant A/G snv 0.20 1
rs16896923
ZNRD1ASP ; ETF1P1
1.000 0.120 6 30032910 non coding transcript exon variant T/C snv 5.0E-02 1
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 2
rs11228565 0.882 0.160 11 69211113 regulatory region variant G/A snv 0.16 2
rs1154865 0.882 0.160 12 73596057 intergenic variant C/G snv 0.22 2
rs1327301 0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29 2
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 2
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 2
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 2
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 2
rs3123078 0.882 0.160 10 46070851 regulatory region variant G/A snv 0.55 2
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 2
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 2
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 2
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 2
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 2
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 2