Variant (rsID / SNP)

rs121909607

rs121909607 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGA. Location: chromosome 4, position 155,510,665. Clinical significance in the table: Pathogenic.

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Reference-table entries

FGAPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 4:155510665
Cytoband: 4q31.3
HGVS: NM_021871.4(FGA):c.104G>A (p.Arg35His)
Allele change: Missense_R35H

Associated conditions / phenotypes

Dysfibrinogenemia|Abnormal bleeding|Hypofibrinogenemia|Familial dysfibrinogenemia

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.