Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 22
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs2735383 0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs150766139 0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 13
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs1864183 0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs1665650 0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs989902 0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs2494938 0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs28366003 0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs59336 0.776 0.160 12 114678547 intron variant T/A;G snv 0.49 10
rs115160714 0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs80359601 0.807 0.360 13 32340890 frameshift variant -/A;NNNNNNNN ins 4.1E-06 8
rs6877842 0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs769412 0.851 0.200 12 68839435 synonymous variant A/G snv 5.5E-02 7.5E-02 6
rs5744455 0.882 0.160 5 140633722 upstream gene variant G/A;T snv 5
rs13078 0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs2230600 0.827 0.160 4 86769845 missense variant A/G snv 0.18 0.14 5
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs4253211 0.882 0.240 10 49470271 missense variant C/G;T snv 7.1E-02; 2.0E-05 3
rs11191865 0.925 0.160 10 103913084 intron variant G/A snv 0.44 3