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: rs137854609
rs137854609
SCN5A
3 0.882 0.120 3 38581170 missense variant C/A;T snv 7.9E-05 0.700 1.000 21 1998 2016