Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs3734091 0.689 0.280 5 83204915 missense variant G/T snv 2.3E-02 1.4E-02 19
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs3212948 0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs843720 0.752 0.280 2 54283523 intron variant T/G snv 0.52 10