Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12449964 1.000 0.040 17 17641390 regulatory region variant C/T snv 0.36 2
rs230119 1.000 0.080 9 119152945 downstream gene variant C/A;T snv 2
rs3851059 10 80270902 downstream gene variant G/A snv 0.27 2
rs4932370 1.000 0.080 15 90861475 intergenic variant G/A;C snv 2
rs4959130 1.000 0.080 6 1356681 intergenic variant G/A snv 9.8E-02 2
rs556621 1.000 6 44626422 intergenic variant T/G snv 0.73 2
rs10123021 9 100689786 regulatory region variant G/A;T snv 1
rs10890917 11 108988857 intergenic variant C/A;G snv 3.5E-02 1
rs11044400 12 19033113 intergenic variant C/T snv 0.13 1
rs112896372 5 3756587 intergenic variant T/C;G snv 1
rs11670734 19 29580124 intergenic variant C/G snv 0.63 1
rs11681884 2 113090051 downstream gene variant C/T snv 0.21 1
rs12417971 11 69202341 intergenic variant C/T snv 6.4E-02 1
rs12442374 15 56012299 intergenic variant C/G;T snv 1
rs12646447 4 110778170 intergenic variant T/C snv 0.15 1
rs1564060 14 84159449 intergenic variant A/G snv 0.68 1
rs17329620 12 87757000 upstream gene variant A/C;G snv 0.11 1
rs1767788 6 44627656 regulatory region variant C/T snv 0.75 1
rs1906599 4 110791530 upstream gene variant T/C snv 0.67 1
rs1937787 1 80373593 non coding transcript exon variant T/C snv 0.23 1
rs1952706 14 36205321 intergenic variant C/G;T snv 1
rs225132 1 8035440 intron variant T/G snv 0.27 1
rs229961 5 57690889 regulatory region variant T/C snv 0.87 1
rs248812 12 97667368 intergenic variant C/A snv 0.74 1
rs2787417 14 36182597 intergenic variant T/C snv 0.66 1