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Variant (rsID / SNP)

rs1077126

OR52B6

rs1077126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52B6. Location: chromosome 11, position 5,602,275. The table records no clinical significance for this variant.

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Reference-table entries

OR52B6Not classified
Variant type
missense_variant
Chromosome / position
11:5602275
HGVS
NM_001005162.2,c.169A>G,p.Thr57Ala
Allele change
Missense_T57A

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.