Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs6857 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs769449 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 8
rs157582 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 5
rs117905930 1.000 0.080 9 88973603 intron variant C/A;T snv 2
rs147906088 1.000 0.080 7 54496119 intergenic variant C/A;T snv 2
rs56214552 1.000 0.080 8 93011994 intron variant T/G snv 0.24 2
rs62187521 1.000 0.080 20 959154 3 prime UTR variant C/T snv 4.8E-03 2
rs6479525 1.000 0.080 9 90331096 intron variant G/A snv 0.44 2
rs72639058 1.000 0.080 1 13913797 intron variant C/A;T snv 2