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: rs672601245
rs672601245
1 1.000 0.120 X 134500026 splice acceptor variant ATA/TTT mnv 0.700 0
dbSNP: rs137852490
rs137852490
1 1.000 0.120 X 134500030 missense variant C/G snv 0.800 1.000 15 1983 2014
dbSNP: rs387906428
rs387906428
1 1.000 0.120 X 134500063 stop lost AATACAAAGCCTAAGATGAGA/- delins 0.700 0