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: rs781140785
rs781140785
KCNH2
2 0.925 0.040 7 150952801 missense variant C/T snv 1.2E-05 4.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs78247304
rs78247304
KCNH7
2 0.925 0.040 2 162446391 missense variant C/T snv 7.6E-05 6.4E-04 0.010 1.000 1 2014 2014