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Variant (rsID / SNP)

rs4936845

OR6M1

rs4936845 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6M1. Location: chromosome 11, position 123,676,231. The table records no clinical significance for this variant.

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Reference-table entries

OR6M1Not classified
Variant type
missense_variant
Chromosome / position
11:123676231
HGVS
NM_001005325.1,c.827C>A,p.Thr276Lys
Allele change
Missense_T276K

Public references

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