Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1557036768
rs1557036768
0.708 0.320 X 53647390 missense variant C/T snv
CUI: C1837404
Disease: High, narrow palate
High, narrow palate
0.700 0
dbSNP: rs1569509136
rs1569509136
0.708 0.400 X 53647576 splice acceptor variant T/C snv
CUI: C1837404
Disease: High, narrow palate
High, narrow palate
0.700 0