Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6009
F5
1.000 0.080 1 169529596 intron variant T/A;C snv 0.94 3
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 3
rs6427196
F5
1.000 0.080 1 169511985 3 prime UTR variant C/G;T snv 3
rs2038024 1.000 0.080 1 169486744 non coding transcript exon variant C/A snv 0.88 2