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Variant (rsID / SNP)

rs7936512

OR52N4

rs7936512 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52N4. Location: chromosome 11, position 5,776,287. The table records no clinical significance for this variant.

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Reference-table entries

OR52N4Not classified
Variant type
missense_variant
Chromosome / position
11:5776287
HGVS
NM_001005175.5,c.317C>T,p.Thr106Ile
Allele change
Missense_T106I

Public references

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