Variant (rsID / SNP)

rs4237768

rs4237768 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52L1. Location: chromosome 11, position 6,007,272. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

OR52L1Not classified

Variant type: missense_variant
Chromosome / position: 11:6007272
HGVS: NM_001005173.3,c.889T>C,p.Trp297Arg
Allele change: Missense_W297R

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.