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Variant (rsID / SNP)

rs1966836

OR1S1

rs1966836 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR1S1. Location: chromosome 11, position 57,982,229. The table records no clinical significance for this variant.

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Reference-table entries

OR1S1Not classified
Variant type
missense_variant
Chromosome / position
11:57982229
HGVS
NM_001004458.2,c.13A>G,p.Ser5Gly
Allele change
Missense_S5G

Public references

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