Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 5
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs6834555 0.882 0.200 4 10060702 regulatory region variant G/A snv 0.74 4
rs714873 0.882 0.200 4 10057994 upstream gene variant G/A snv 0.74 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs4605275 1.000 0.080 19 44835236 intergenic variant T/C snv 0.69 3
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 2
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 2
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 2
rs10405693 1.000 0.080 19 44823407 downstream gene variant C/T snv 0.28 1
rs10792832 1.000 0.080 11 86156833 downstream gene variant A/G snv 0.70 1
rs10850408 1.000 0.080 12 114942588 intergenic variant C/T snv 0.31 1
rs11827324 1.000 0.080 11 60332439 upstream gene variant A/G snv 0.30 1
rs12334143 1.000 0.080 7 85553700 regulatory region variant T/C snv 0.33 1
rs12425791 0.882 0.120 12 674318 downstream gene variant G/A;C snv 1
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 1
rs12798898 1.000 0.080 11 85948537 intergenic variant A/G snv 1.0E-01 1
rs13178362 1.000 0.080 5 30178906 intergenic variant T/C snv 0.17 1
rs13241213 1.000 0.080 7 50255260 intron variant C/G;T snv 1