Variant (rsID / SNP)

rs12577167

rs12577167 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51I2, OR51B5. Location: chromosome 11, position 5,475,118. The table records no clinical significance for this variant.

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Reference-table entries

OR51I2Not classified

Variant type: missense_variant
Chromosome / position: 11:5475118
HGVS: NM_001004754.3,c.400A>G,p.Thr134Ala
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.