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: rs1332629192
rs1332629192
ALB
7 0.851 0.200 4 73404374 missense variant C/T snv 0.020 1.000 2 2007 2009
dbSNP: rs58624704
rs58624704
ALB
2 0.925 0.200 4 73410325 missense variant G/A snv 8.0E-06 3.5E-05 0.010 1.000 1 2017 2017