Variant (rsID / SNP)

rs11880184

rs11880184 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10H4. Location: chromosome 19, position 16,060,658. The table records no clinical significance for this variant.

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Reference-table entries

OR10H4Not classified

Variant type: missense_variant
Chromosome / position: 19:16060658
HGVS: NM_001004465.1,c.841A>G,p.Thr281Ala
Allele change: Missense_T281A

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.