Variant (rsID / SNP)

rs9822460

rs9822460 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5K4. Location: chromosome 3, position 98,073,313. The table records no clinical significance for this variant.

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Reference-table entries

OR5K4Not classified

Variant type: missense_variant
Chromosome / position: 3:98073313
HGVS: NM_001005517.1,c.616A>G,p.Ile206Val
Allele change: Missense_I206V

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.