Variant (rsID / SNP)

rs121913090

rs121913090 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGG. Location: chromosome 4, position 155,527,985. Clinical significance in the table: other.

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Reference-table entries

FGGOther

Clinical significance (as recorded): other
Variant type: single nucleotide variant
Chromosome / position: 4:155527985
Cytoband: 4q32.1
HGVS: NM_021870.2(FGG):c.1001A>T (p.Asn334Ile)
Allele change: Missense_N334I

Associated conditions / phenotypes

FIBRINOGEN BALTIMORE 3

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.