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Variant (rsID / SNP)

rs7118113

OR51B4

rs7118113 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51B4. Location: chromosome 11, position 5,323,071. The table records no clinical significance for this variant.

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Reference-table entries

OR51B4Not classified
Variant type
missense_variant
Chromosome / position
11:5323071
HGVS
NM_033179.2,c.106G>A,p.Val36Ile
Allele change
Missense_V36I

Public references

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