Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1560814874 4 143528006 missense variant A/C snv 1
rs1562005199 6 69382853 missense variant G/A snv 1
rs1562137453 6 69049307 missense variant T/C snv 1
rs1562308994 6 99446205 missense variant T/C snv 1
rs1562391520 6 99482871 missense variant C/T snv 1
rs1562456317 6 99508705 missense variant A/C snv 1
rs1563293555 8 42930130 missense variant T/G snv 1
rs1563765580 8 92017274 frameshift variant -/A ins 1
rs1564726619 10 69232838 missense variant G/T snv 1
rs1565117343 11 59594048 stop gained G/A snv 1
rs1565272952 11 17145862 splice donor variant C/A snv 1
rs1565798439 12 71610513 missense variant A/G snv 1
rs1566529937 13 114052075 missense variant A/G snv 1
rs1566615893 14 24155442 missense variant A/G snv 1
rs1567280099 16 4697038 frameshift variant -/G delins 1
rs1567547614 16 30668622 missense variant G/A snv 1
rs1567858976 17 32477518 splice region variant CAGA/- delins 1
rs1567966432 18 21383629 missense variant T/G snv 1
rs1568105562 17 44559091 missense variant T/G snv 1
rs1568162263 17 40029767 missense variant G/C snv 1
rs1568383758 19 15255488 missense variant C/A snv 1
rs1569148952 X 37991160 frameshift variant TG/- del 1
rs1569197778 X 55488927 stop gained G/A snv 1
rs1569405174 X 110317618 frameshift variant G/- delins 1
rs193922466 Y 634687 missense variant A/G snv 1