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: rs104894073
rs104894073
GATA4
8 0.827 0.080 8 11750213 missense variant G/A;C;T snv 0.020 1.000 2 2012 2019
dbSNP: rs754369510
rs754369510
NUP214
3 0.925 0.040 9 131134988 missense variant A/G snv 4.0E-06 0.010 1.000 1 2012 2012