Variant (rsID / SNP)

rs2070011

rs2070011 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGA. Location: chromosome 4, position 155,511,897. Clinical significance in the table: Benign.

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Reference-table entries

FGABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:155511897
Cytoband: 4q31.3
HGVS: NM_021871.3(FGA):c.-58A>G
Allele change: Silent

Associated conditions / phenotypes

Familial visceral amyloidosis, Ostertag type|Congenital afibrinogenemia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.