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: rs74315431
rs74315431
VAPB
15 0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 0.820 1.000 15 2004 2016
dbSNP: rs281875284
rs281875284
VAPB
2 0.925 0.080 20 58418289 missense variant C/T snv 0.800 1.000 4 2004 2012