Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019997 4 136127444 intron variant C/T snv 0.47 1
rs1002226 11 17384070 downstream gene variant C/T snv 0.69 1
rs1003081 11 119043282 upstream gene variant C/T snv 0.38 1
rs10060123 5 126348218 intron variant C/A snv 0.22 1
rs1006353 13 27473132 regulatory region variant A/G snv 0.64 1
rs10091344 8 34274557 intron variant G/A;C snv 1
rs10102172 8 76326157 intergenic variant A/C;G snv 1
rs1011407 2 60438633 intron variant A/G snv 7.7E-02 1
rs10160769 11 76763783 intron variant G/C snv 0.35 1
rs10169594 2 41410548 intergenic variant T/C;G snv 1
rs10172678 2 59067423 intron variant T/C snv 0.63 1
rs10179086 2 231879499 intergenic variant T/C snv 0.29 1
rs10248288 7 27212157 intron variant C/G snv 0.40 1
rs1031670 18 63056554 intergenic variant T/C snv 0.57 1
rs1035491 5 64666350 regulatory region variant A/G snv 0.42 1
rs1037702 4 179246870 intergenic variant G/A snv 0.67 1
rs10427204 2 204239930 upstream gene variant G/A snv 0.43 1
rs10440098 3 20537506 intron variant T/C snv 0.35 1
rs10495537 2 6554387 intergenic variant C/T snv 0.25 1
rs10497882 2 206368391 intergenic variant T/C snv 0.21 1
rs10499276 6 153988673 intergenic variant C/T snv 0.11 1
rs10742752 11 45416824 intron variant T/C snv 0.68 1
rs10744146 12 17059947 intergenic variant G/A snv 0.47 1
rs10757826 9 29270226 intergenic variant G/A snv 0.33 1
rs10760277 9 123331720 intergenic variant C/T snv 0.33 1