Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10138053 14 51148434 intergenic variant T/C snv 0.74 1
rs10510776 3 55162885 downstream gene variant C/A snv 0.44 1
rs11027001 11 23133679 intergenic variant T/C snv 0.43 1
rs11079867 17 49277423 intron variant A/C snv 0.53 1
rs12431939 14 51225981 regulatory region variant G/A snv 0.16 1
rs12539089 7 142798609 upstream gene variant C/A snv 0.47 1
rs12580194 12 55302774 intergenic variant G/A snv 0.31 1
rs12588488 14 51193499 intergenic variant C/A;T snv 1
rs1506403 7 143053854 downstream gene variant C/T snv 0.31 1
rs1577074 10 118223544 intergenic variant A/G snv 0.16 1
rs17837474 7 142669182 upstream gene variant A/G snv 0.13 1
rs17837475 7 142681397 upstream gene variant C/T snv 6.4E-02 1
rs2063993 7 142847457 intergenic variant T/A;G snv 1
rs2078176 7 142649362 downstream gene variant A/G snv 0.48 1
rs2197159 17 49400273 intron variant C/T snv 0.68 1
rs2584663 17 49390785 intron variant G/A snv 0.36 1
rs2834439 21 34300618 intron variant A/G snv 0.73 1
rs2834440 21 34318199 intron variant G/A snv 0.55 1
rs2834450 21 34329783 intron variant G/A snv 0.72 1
rs2834461 21 34344072 intron variant A/C snv 0.52 1
rs2898857 17 49278661 intron variant G/T snv 0.25 1
rs2999393 14 51188449 intergenic variant G/T snv 0.71 1
rs3007168 14 51141575 intergenic variant G/A snv 0.15 1
rs3134906 7 142807470 downstream gene variant G/A snv 0.56 1
rs3763608 9 69032459 upstream gene variant T/C snv 0.37 1