Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2205960 0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs1234313 0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs16841904 0.807 0.160 1 197732862 intron variant C/T snv 0.18 6
rs6659932 0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 4
rs3790567 0.851 0.240 1 67356694 intron variant A/G snv 0.61 4
rs2300747 0.882 0.200 1 116561593 intron variant A/G snv 0.19 3
rs2843403 0.882 0.200 1 2597658 intron variant T/C snv 0.54 3
rs10889681 0.925 0.160 1 67333487 intron variant T/A;C snv 2
rs17129789 0.925 0.080 1 67324915 intron variant T/C snv 0.17 2
rs17641524 0.925 0.120 1 197735587 splice region variant C/G;T snv 4.0E-06; 0.17 2
rs4620530 0.925 0.080 1 239900521 intron variant T/G snv 0.44 2
rs6679356 0.925 0.200 1 67354511 intron variant C/T snv 0.75 2
rs11209050 1.000 0.080 1 67326053 intron variant A/C snv 0.68 1
rs11209051 1.000 0.080 1 67333212 intron variant C/T snv 0.73 1
rs1539414 1.000 0.080 1 197774376 intron variant G/A snv 0.23 1
rs1572037 1.000 0.080 1 3337805 intron variant T/A;C snv 0.33 1
rs1999527 1.000 0.080 1 3339544 intron variant C/A;T snv 1
rs2488393 1.000 0.080 1 197753110 intron variant C/T snv 0.23 1
rs4648379 1.000 0.080 1 3344952 intron variant C/T snv 0.31 1
rs4648477 1.000 0.080 1 3335411 intron variant G/A snv 0.33 1
rs4648478 1.000 0.080 1 3335443 intron variant C/T snv 0.33 1
rs56194793 1.000 0.080 1 67324915 intron variant T/C snv 1
rs72678531 1.000 0.080 1 67332762 intron variant T/C snv 0.17 1