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: rs104893749
rs104893749
MYL3
2 0.925 0.080 3 46859495 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.800 1.000 4 1996 2013