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Variant (rsID / SNP)

rs1995158

OR52H1

rs1995158 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52H1. Location: chromosome 11, position 5,566,030. The table records no clinical significance for this variant.

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Reference-table entries

OR52H1Not classified
Variant type
missense_variant
Chromosome / position
11:5566030
HGVS
NM_001005289.5,c.706T>C,p.Cys236Arg
Allele change
Missense_C242R

Public references

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