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: rs767169659
rs767169659
MYLK
1 1.000 0.040 3 123733800 missense variant G/A snv 1.2E-05 0.010 1.000 1 2015 2015