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: rs762114560
rs762114560
ACADM
1 1.000 0.080 1 75732886 missense variant C/T snv 7.2E-05 7.0E-05 0.700 1.000 5 2006 2012