Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12515541 5 57799184 intergenic variant G/T snv 0.59 1
rs12574332 11 122650415 regulatory region variant C/T snv 0.13 1
rs1265842 10 28635972 intergenic variant T/A;C snv 0.56 1
rs13001283 2 126425877 intergenic variant G/A snv 0.14 1
rs13040824 20 2245223 intron variant G/A snv 0.22 1
rs13094615 3 47493431 downstream gene variant T/C;G snv 1
rs1322639 6 169187008 upstream gene variant G/A snv 0.73 1
rs138475089 7 100899019 upstream gene variant -/TA delins 1
rs143112823 3 154990178 intergenic variant G/A snv 8.4E-02 1
rs1468520 7 7251101 upstream gene variant A/G;T snv 1
rs148387718 6 9445767 intergenic variant C/G;T snv 1
rs148753653 16 20218853 intergenic variant A/G snv 3.8E-03 1
rs148772934 11 44984130 regulatory region variant T/G snv 3.8E-04 1
rs150834401 4 102243067 intergenic variant C/T snv 3.2E-02 1
rs1607644 2 34454559 intron variant G/A snv 0.27 1
rs169287 6 27886982 downstream gene variant C/A snv 0.16 1
rs1706003 3 194579238 upstream gene variant G/A;T snv 1
rs17454517 7 50848079 upstream gene variant A/G;T snv 1
rs1761870 6 116943822 intergenic variant G/A snv 0.78 1
rs17875419 10 114037712 intergenic variant G/- delins 0.14 1
rs1821295 19 32099867 upstream gene variant C/T snv 0.77 1
rs182662555 1 95823780 intergenic variant T/C snv 2.5E-04 1
rs187222839 11 98073424 intergenic variant T/C snv 1.6E-03 1
rs1886914 1 118998829 downstream gene variant C/A;G snv 1
rs1947228 7 96832337 regulatory region variant T/A;C snv 1