Variant (rsID / SNP)

rs11033352

rs11033352 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51C1P, OR51E2. Location: chromosome 11, position 4,712,353. The table records no clinical significance for this variant.

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Reference-table entries

OR51C1PNot classified

Variant type: missense_variant
Chromosome / position: 11:4712353
HGVS: NM_001396051.1,c.574A>G,p.Thr192Ala
Allele change: Silent

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.