Variant (rsID / SNP)

rs1536929

rs1536929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR1B1. Location: chromosome 9, position 125,391,369. The table records no clinical significance for this variant.

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Reference-table entries

OR1B1Not classified

Variant type: missense_variant
Chromosome / position: 9:125391369
HGVS: NM_001004450.2,c.443T>C,p.Leu148Ser
Allele change: Missense_L149S

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.