Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10211665 1.000 0.120 2 46298957 intron variant T/C snv 0.58 1
rs11125068 1.000 0.120 2 46300677 intron variant A/G snv 0.62 1
rs11684885 1.000 0.120 2 46306413 intron variant T/C;G snv 1
rs11689011 1.000 0.120 2 46314037 intron variant T/A;C;G snv 1
rs11894252 0.925 0.120 2 46306237 intron variant T/A;C;G snv 1
rs17034950 1.000 0.120 2 46311655 intron variant G/A snv 0.25 1
rs1867784 1.000 0.120 2 46307081 intron variant T/C snv 0.40 1
rs1867785 1.000 0.120 2 46307199 intron variant A/G snv 0.52 1
rs1867787 1.000 0.120 2 46298252 intron variant G/C;T snv 1
rs2034327 1.000 0.120 2 46321901 intron variant G/C snv 0.59 1
rs2044456 1.000 0.120 2 46319177 intron variant A/G snv 0.26 1
rs2121266 1.000 0.120 2 46308785 intron variant C/A snv 0.61 1
rs2346417 1.000 0.120 2 46301822 intron variant T/A snv 0.39 1
rs4952818 1.000 0.120 2 46309917 intron variant C/T snv 0.39 1
rs4953340 1.000 0.120 2 46320925 intron variant C/A;G snv 1
rs7579899 0.925 0.120 2 46310465 intron variant A/G snv 0.52 1
rs9973653 1.000 0.120 2 46320970 intron variant G/T snv 0.42 1