Variant (rsID / SNP)

rs5006888

rs5006888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51B6, OR51B5. Location: chromosome 11, position 5,373,114. The table records no clinical significance for this variant.

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Reference-table entries

OR51B6Not classified

Variant type: missense_variant
Chromosome / position: 11:5373114
HGVS: NM_001004750.1,c.377G>A,p.Ser126Asn
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.