Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1982094 8 129612570 intron variant C/T snv 4.8E-02 5
rs397731840 8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 5
rs10098310 8 129601368 intron variant G/A;T snv 2
rs1433578 8 129588843 intron variant T/C snv 9.1E-02 1
rs2163950 8 129585339 intron variant C/A snv 9.2E-02 1
rs55964818 8 129593625 intron variant T/C snv 0.56 1
rs9297779 8 128973991 intron variant C/G;T snv 1