Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs886041065
rs886041065
ASXL2
43 0.677 0.600 2 25743913 frameshift variant G/- delins 0.700 0
dbSNP: rs886041066
rs886041066
ASXL2
1 1.000 2 25744255 frameshift variant -/C delins 0.700 0
dbSNP: rs886041067
rs886041067
ASXL2
1 1.000 2 25750328 frameshift variant GTTG/- delins 0.700 0
dbSNP: rs886041068
rs886041068
ASXL2
1 1.000 2 25743865 frameshift variant G/- delins 0.700 0
dbSNP: rs886041069
rs886041069
ASXL2
1 1.000 2 25743363 frameshift variant TCCC/- delins 0.700 0
dbSNP: rs886041070
rs886041070
ASXL2
1 1.000 2 25750268 stop gained C/A snv 0.700 0