Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs147495977 1.000 0.120 5 78885823 missense variant G/A;C snv 2.5E-04 1.0E-03 1
rs1484763838 1.000 0.120 5 78964597 missense variant A/C;T snv 7.0E-06 1
rs1554032090 1.000 0.120 5 78984956 missense variant A/C;G;T snv 1
rs1554032094 1.000 0.120 5 78984960 stop gained G/A snv 1
rs1554032095 1.000 0.120 5 78984961 missense variant G/C snv 1
rs1554032099 1.000 0.120 5 78984968 stop gained G/A;T snv 1
rs1554032110 1.000 0.120 5 78984975 frameshift variant TGCAC/- del 1
rs1554032118 1.000 0.120 5 78984985 frameshift variant -/T delins 1
rs1554032122 1.000 0.120 5 78984992 frameshift variant T/- del 1
rs1554032129 1.000 0.120 5 78984996 missense variant A/G snv 1
rs1554032131 1.000 0.120 5 78985001 frameshift variant TC/- del 1
rs1554032134 1.000 0.120 5 78985006 frameshift variant GAGCACC/- del 1
rs1554032145 1.000 0.120 5 78985017 frameshift variant GCCGCCAGCG/- delins 1
rs1554032153 1.000 0.120 5 78985030 frameshift variant G/- del 1
rs1554032155 1.000 0.120 5 78985034 frameshift variant AGGTGCGG/- del 1
rs1554032160 1.000 0.120 5 78985035 frameshift variant -/CGTGCGG delins 1
rs1554032196 1.000 0.120 5 78985059 frameshift variant -/T ins 1
rs1554032216 1.000 0.120 5 78985089 missense variant C/T snv 1
rs1554032217 1.000 0.120 5 78985092 missense variant C/T snv 1
rs1554032220 1.000 0.120 5 78985097 missense variant A/G snv 1
rs1554032222 1.000 0.120 5 78985100 stop gained A/T snv 1
rs1554032243 1.000 0.120 5 78985126 frameshift variant GGCCCCGG/- del 1
rs1554032252 1.000 0.120 5 78985135 frameshift variant G/- del 1
rs1554069659 1.000 0.120 5 78780407 missense variant G/C snv 1
rs1554069660 1.000 0.120 5 78780422 frameshift variant G/- del 1