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: rs1205538057
rs1205538057
ACE
5 0.827 0.200 17 63483937 missense variant A/G snv 4.0E-06 0.020 1.000 2 2008 2009
dbSNP: rs757110
rs757110
ABCC8
6 0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 0.010 < 0.001 1 2010 2010