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Variant (rsID / SNP)

rs10896271

OR8K1

rs10896271 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8K1. Location: chromosome 11, position 56,113,575. The table records no clinical significance for this variant.

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Reference-table entries

OR8K1Not classified
Variant type
missense_variant
Chromosome / position
11:56113575
HGVS
NM_001002907.1,c.61A>G,p.Met21Val
Allele change
Missense_M21V

Public references

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