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Variant (rsID / SNP)

rs6063

FGG

rs6063 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGG. Location: chromosome 4, position 155,530,877. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FGGConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
4:155530877
Cytoband
4q32.1
HGVS
NM_021870.3(FGG):c.571G>A (p.Gly191Arg)
Allele change
Missense_G191R

Associated conditions / phenotypes

Fibrinogen Milano XII, digenic|Hypofibrinogenemia|Congenital afibrinogenemia|Familial dysfibrinogenemia

Public references

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