Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2999393 14 51188449 intergenic variant G/T snv 0.71 1
rs3007168 14 51141575 intergenic variant G/A snv 0.15 1
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 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
rs4121859 11 95444976 regulatory region variant C/T snv 0.20 1
rs4281045 7 142810692 downstream gene variant C/A snv 0.20 1
rs450533 4 106909104 intron variant T/C snv 0.36 1
rs4553443 12 54929761 intergenic variant T/A;G snv 1
rs4594175 14 51139823 regulatory region variant C/A snv 0.33 1
rs4794031 17 49264791 intron variant C/A;T snv 1
rs4817642 21 34312702 intron variant G/A snv 0.48 1
rs5029614 6 18100143 intergenic variant A/G snv 0.32 1
rs534126 7 143224141 non coding transcript exon variant C/G;T snv 1
rs538592 11 95367983 regulatory region variant C/T snv 0.75 1
rs62355900 1.000 0.040 5 56756868 regulatory region variant T/C snv 0.15 1
rs659119 6 149212011 intergenic variant C/T snv 0.17 1
rs6946770 7 142693973 upstream gene variant A/G;T snv 1
rs6975391 7 142662001 upstream gene variant T/A;C;G snv 1
rs7148539 14 51168554 regulatory region variant C/A;T snv 1
rs8129326 21 34440329 intergenic variant A/G snv 1
rs9323205 14 51119749 regulatory region variant A/G snv 0.21 1
rs9376307 6 137962128 intron variant C/T snv 0.28 1
rs9599474 13 34721318 intergenic variant A/G snv 0.14 1
rs971535 11 23123974 regulatory region variant C/T snv 0.46 1