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: rs132630286
rs132630286
PLP1 ; RAB9B
2 0.925 0.120 X 103788475 missense variant G/T snv 0.700 0
dbSNP: rs132630293
rs132630293
PLP1 ; RAB9B
2 0.925 0.120 X 103789361 missense variant C/T snv 0.700 0