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Variant (rsID / SNP)

rs3813355

TAAR5

rs3813355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAAR5. Location: chromosome 6, position 132,910,612. The table records no clinical significance for this variant.

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Reference-table entries

TAAR5Not classified
Variant type
synonymous_variant
Chromosome / position
6:132910612
HGVS
NM_001389527.1,c.214C>T,p.Leu72Leu
Allele change
Synonymous_L72L

Public references

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