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Variant (rsID / SNP)

rs10768448

OR51L1

rs10768448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51L1. Location: chromosome 11, position 5,020,799. The table records no clinical significance for this variant.

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Reference-table entries

OR51L1Not classified
Variant type
missense_variant
Chromosome / position
11:5020799
HGVS
NM_001004755.2,c.587C>T,p.Thr196Ile
Allele change
Missense_T196I

Public references

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