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: rs1251794140
rs1251794140
MOG
1 1.000 0.080 6 29659504 missense variant C/T snv 8.1E-06 7.0E-06 0.020 1.000 2 2004 2005