Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10068807 5 55581157 intergenic variant A/G snv 0.70 1
rs10917220 1 22356912 intergenic variant T/C snv 0.65 1
rs11128264 3 72343159 intergenic variant C/T snv 0.55 1
rs11160601 14 100720304 regulatory region variant C/G;T snv 1
rs11243202 6 7718832 intergenic variant T/C snv 0.39 1
rs11874191 18 38584120 intergenic variant C/T snv 0.66 1
rs11944404 4 144749719 intron variant T/C snv 0.39 1
rs1228024 11 47929801 regulatory region variant C/A snv 0.56 1
rs12409277 1 3041036 intergenic variant T/C snv 0.17 1
rs12694002 2 204517128 intergenic variant C/G snv 9.0E-02 1
rs138525295 6 128810270 intergenic variant T/C snv 3.1E-02 1
rs139055636 9 102796618 regulatory region variant C/A;T snv 1
rs1452822 8 77226098 intergenic variant T/A snv 0.23 1
rs1541597 12 109607113 intergenic variant G/T snv 0.20 1
rs1544459 7 77788267 intergenic variant T/C snv 0.55 1
rs1662835 4 81251295 intergenic variant T/C snv 0.44 1
rs1682093 2 22551319 downstream gene variant C/T snv 0.95 1
rs17246129 2 226395248 intergenic variant G/A;T snv 1
rs183041 5 177099269 downstream gene variant G/A snv 0.70 1
rs2345701 7 46595000 intergenic variant C/G snv 0.52 1
rs2408508 12 46336817 intergenic variant T/A;C snv 1
rs2474944 1 118342903 intergenic variant T/A;C;G snv 1
rs397858888 18 60165624 downstream gene variant C/-;CC;CCC delins 1
rs401746 6 160319208 intergenic variant T/C snv 0.46 1
rs4819021 21 45047012 intergenic variant T/C snv 0.59 1