Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554700718
HNRNPK
0.658 0.360 9 83975540 non coding transcript exon variant T/C snv 59
rs886041065
ASXL2
0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1565307564
TMEM258 ; MYRF
0.807 0.120 11 61783599 missense variant A/G snv 7
rs114878910
EXOSC3
0.882 0.080 9 37784894 stop gained G/A;C snv 8.6E-06; 3.1E-04 4