Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Mackenzie's Mission_Reproductive Carrier Screening

Gene: FGB

Green List (high evidence)

FGB (fibrinogen beta chain)
EnsemblGeneIds (GRCh38): ENSG00000171564
EnsemblGeneIds (GRCh37): ENSG00000171564
OMIM: 134830, Gene2Phenotype
FGB is in 7 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Afibrinogenemia, congenital, 202400 (3)
OMIM
134830
Clinvar variants
Variants in FGB
Penetrance
None
Panels with this gene

History Filter Activity

19 Apr 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: FGB was added gene: FGB was added to Mackenzie's Mission_Reproductive Carrier Screening. Sources: Mackenzie's Mission,Expert Review Green Mode of inheritance for gene: FGB was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FGB were set to Afibrinogenemia, congenital, 202400 (3)