Variant (rsID / SNP)

rs17511668

rs17511668 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to N4BP2. Location: chromosome 4, position 40,103,767. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

N4BP2Not classified

Variant type: missense_variant
Chromosome / position: 4:40103767
HGVS: NM_018177.6,c.302G>T,p.Ser101Ile
Allele change: Missense_S101I

Associated conditions / phenotypes

Nasopharyngeal Carcinoma

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.