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AFM

Synonyms
ALB2, ALBA, ALF
External resources
Summary
This gene is a member of the albumin gene family, which is comprised of four genes that localize to chromosome 4 in a tandem arrangement. These four genes encode structurally-related serum transport proteins that are known to be evolutionarily related. The protein encoded by this gene is regulated developmentally, expressed in the liver and secreted into the bloodstream.

Variant counts

The variants found in rare patients tested by 3billion are classified and counted according to ACMG guidelines. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc) are excluded.

Pathogenic
0
Likely pathogenic
0
VUS
7,905
Likely benign
5,712
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on AFM gene.

Phenotype class
Patients in 3billion (%)

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