Variant (rsID / SNP)

rs484373

rs484373 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGL1. Location: chromosome 8, position 17,743,020. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FGL1Not classified

Variant type: missense_variant
Chromosome / position: 8:17743020
HGVS: NM_004467.4,c.44C>T,p.Thr15Ile
Allele change: Missense_T15I

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.