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: rs2857766
rs2857766
MOG
4 0.882 0.120 6 29666226 missense variant G/C snv 0.22 0.19 0.050 1.000 5 2002 2013
dbSNP: rs3130253
rs3130253
MOG
3 0.925 0.120 6 29666235 missense variant A/G;T snv 0.95; 4.1E-06 0.040 1.000 4 1997 2020
dbSNP: rs112913018
rs112913018
MOG
1 1.000 0.080 6 29670324 missense variant T/A;C snv 5.7E-04; 2.8E-03 0.010 1.000 1 2002 2002