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: rs121912515
rs121912515
KCNH2
2 0.925 0.120 7 150974720 missense variant G/A;C;T snv 0.700 0
dbSNP: rs137854619
rs137854619
SCN5A
2 0.925 0.120 3 38550917 missense variant C/T snv 2.7E-04 7.7E-05 0.700 0