Variant (rsID / SNP)

rs25882

rs25882 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSF2. Location: chromosome 5, position 131,411,460. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CSF2Not classified

Variant type: missense_variant
Chromosome / position: 5:131411460
HGVS: NM_000758.4,c.350T>C,p.Ile117Thr
Allele change: Missense_I117T

Associated conditions / phenotypes

Cytokine Deficiency|Adenocarcinoma

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.