ALB, albumin, 213

N. diseases: 1198; N. variants: 21
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs75002628
rs75002628
0.925 0.080 4 73412007 missense variant G/A;C snv 7.2E-05
Hyperthyroxinemia, Familial Dysalbuminemic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases 0.820 1.000 6 1994 2019
dbSNP: rs77892378
rs77892378
1.000 0.080 4 73406760 missense variant T/C;G snv
Hyperthyroxinemia, Familial Dysalbuminemic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases 0.800 1.000 4 1994 1998