Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72761442 1.000 0.040 5 61400496 intron variant A/G snv 0.18 2
rs13179617 5 61527343 intron variant G/T snv 0.38 1
rs10223052 5 61504509 intron variant A/G snv 0.73 1
rs78922867 5 61501931 intron variant G/C snv 8.5E-03 1
rs142089946 1.000 0.040 5 61495766 intron variant C/G snv 3.3E-02 1
rs7709645 1.000 0.040 5 61435631 intron variant G/A;C snv 1
rs7719676 1.000 0.040 5 61441122 intron variant A/G;T snv 1
rs4490539 5 61389930 intron variant A/G snv 0.31 1
rs74419120 5 61447591 intron variant C/G;T snv 1
rs74320437 5 61447778 intron variant C/T snv 0.17 1
rs7714712 5 61436725 intron variant C/A snv 0.37 1
rs7720894 5 61438106 intron variant G/C snv 0.63 1
rs6449533 5 61426817 intron variant T/C snv 0.36 1