Variant (rsID / SNP)

rs379707

rs379707 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FYB1. Location: chromosome 5, position 39,119,723. The table records no clinical significance for this variant.

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Reference-table entries

FYB1Not classified

Variant type: missense_variant
Chromosome / position: 5:39119723
HGVS: NM_001243093.2,c.2182G>T,p.Val728Phe
Allele change: Missense_V682F

Associated conditions / phenotypes

Autoimmune Disease|Lupus Erythematosus

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.