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Variant (rsID / SNP)

rs7397032

OR56B1

rs7397032 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR56B1. Location: chromosome 11, position 5,758,062. The table records no clinical significance for this variant.

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Reference-table entries

OR56B1Not classified
Variant type
missense_variant
Chromosome / position
11:5758062
HGVS
NM_001005180.3,c.316T>C,p.Cys106Arg
Allele change
Missense_C106R

Public references

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