Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 1
rs10440635 1.000 0.040 5 40490688 intron variant G/A snv 0.56 1
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
rs10957979 1.000 0.080 8 80377552 intron variant A/G snv 0.61 1
rs11217036 11 118805063 intergenic variant C/G;T snv 1
rs11255968 10 8894199 upstream gene variant C/T snv 9.3E-02 1
rs11464691 17 40614389 intergenic variant -/A delins 0.68 1
rs12543811 1.000 0.080 8 80366650 intron variant G/A snv 0.62 1
rs13153019 5 177355217 upstream gene variant T/C snv 0.21 1
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 1
rs13384448 2 227843146 intergenic variant C/T snv 0.67 1
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 1
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 1
rs1444789 10 9022398 intergenic variant T/C snv 0.23 1
rs150254607 4 122532955 intergenic variant -/TAT ins 4.9E-02 1
rs1505992 5 40498475 intron variant A/T snv 0.61 1
rs1663687 1.000 0.080 10 9012824 intergenic variant G/A snv 0.35 1
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 1
rs17664743 7 50214301 intron variant G/A snv 0.24 1
rs1775550 10 9010779 regulatory region variant G/A;C snv 1
rs1794275 1.000 0.120 6 32703471 downstream gene variant G/A snv 0.21 1
rs1814576 5 110824180 intergenic variant T/C snv 7.0E-02 1
rs2030030 3 188076045 intergenic variant T/C snv 0.13 1
rs2095044 9 6192796 upstream gene variant T/C snv 0.64 1