Variant (rsID / SNP)

rs7145814

rs7145814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5AU1. Location: chromosome 14, position 21,623,290. The table records no clinical significance for this variant.

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Reference-table entries

OR5AU1Not classified

Variant type: missense_variant
Chromosome / position: 14:21623290
HGVS: NM_001004731.3,c.742A>G,p.Ile248Val
Allele change: Missense_I299V

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.