Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 4
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 3
rs4712523 0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs6931514 0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs7754840 0.807 0.200 6 20661019 intron variant G/A;C;T snv 3
rs7766070 1.000 0.080 6 20686342 intron variant C/A snv 0.25 3
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 3
rs9368219 1.000 0.080 6 20674460 intron variant C/T snv 0.19 3
rs9465871 0.882 0.120 6 20717024 intron variant T/C snv 0.30 3
rs4712524 0.925 0.120 6 20657634 intron variant A/G snv 0.40 2
rs6456368 1.000 0.080 6 20659575 intron variant T/C snv 0.40 2
rs7741604 0.925 0.120 6 20731293 intron variant A/C;T snv 2
rs7767391 1.000 0.080 6 20725009 intron variant T/C snv 0.28 2
rs9348440 1.000 0.080 6 20641105 intron variant C/T snv 0.13 2
rs1040558 1.000 0.080 6 20713475 intron variant A/G snv 0.19 1
rs10440833 1.000 0.080 6 20687890 intron variant T/A;G snv 0.26 1
rs10946403 1.000 0.080 6 20717173 intron variant A/G snv 0.30 1
rs11753081 1.000 0.080 6 20705359 intron variant T/G snv 0.19 1
rs12111351 1.000 0.080 6 20724327 intron variant T/G snv 0.34 1
rs12664021 1.000 0.080 6 20760849 intron variant C/T snv 0.11 1
rs145494032 1.000 0.080 6 20665715 intron variant -/C delins 4.9E-05 1
rs1569699 1.000 0.080 6 20679079 intron variant T/G snv 0.41 1