Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35261542 1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 3
rs35612982 1.000 0.080 6 20682391 intron variant T/C snv 0.29 2
rs6931514 0.925 0.120 6 20703721 intron variant A/G snv 0.27 2
rs742642 1.000 0.080 6 20664850 intron variant G/A snv 0.21 2
rs7754840 0.807 0.200 6 20661019 intron variant G/A;C;T snv 2
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 2
rs9358356 1.000 0.080 6 20667151 intron variant T/C snv 0.39 2
rs10440833 1.000 0.080 6 20687890 intron variant T/A;G snv 0.26 1
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 1
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 1
rs4712523 0.925 0.120 6 20657333 intron variant A/G snv 0.41 1
rs4712524 0.925 0.120 6 20657634 intron variant A/G snv 0.40 1
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 1
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 1
rs7766070 1.000 0.080 6 20686342 intron variant C/A snv 0.25 1
rs9348440 1.000 0.080 6 20641105 intron variant C/T snv 0.13 1
rs9460550 1.000 0.080 6 20719330 intron variant G/A snv 0.30 1
rs9465871 0.882 0.120 6 20717024 intron variant T/C snv 0.30 1