Variant (rsID / SNP)

rs4407791

rs4407791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2A5. Location: chromosome 7, position 143,748,364. The table records no clinical significance for this variant.

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Reference-table entries

OR2A5Not classified

Variant type: synonymous_variant
Chromosome / position: 7:143748364
HGVS: NM_012365.2,c.870T>C,p.Tyr290Tyr
Allele change: Synonymous_Y290Y

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.