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Variant (rsID / SNP)

rs116908319

OR56A5

rs116908319 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR56A5. Location: chromosome 11, position 5,989,282. The table records no clinical significance for this variant.

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Reference-table entries

OR56A5Not classified
Variant type
missense_variant
Chromosome / position
11:5989282
HGVS
NM_001146033.1,c.443C>T,p.Ala148Val
Allele change
Missense_A148V

Public references

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