Variant (rsID / SNP)

rs4518168

rs4518168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5AC2. Location: chromosome 3, position 97,806,616. The table records no clinical significance for this variant.

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Reference-table entries

OR5AC2Not classified

Variant type: missense_variant
Chromosome / position: 3:97806616
HGVS: NM_054106.1,c.600G>A,p.Met200Ile
Allele change: Missense_M200I

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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