Variant (rsID / SNP)

rs1807757

rs1807757 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5BS1P. Location: chromosome 12, position 48,954,040. The table records no clinical significance for this variant.

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Reference-table entries

OR5BS1PNot classified

Variant type: missense_variant
Chromosome / position: 12:48954040
HGVS: NM_001396061.1,c.376A>G,p.Met126Val

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.