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: rs878855295
rs878855295
SCN5A
1 1.000 0.200 3 38550619 missense variant T/C snv 0.010 1.000 1 2017 2017