Variant (rsID / SNP)

rs7026705

rs7026705 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR13C8. Location: chromosome 9, position 107,331,504. The table records no clinical significance for this variant.

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Reference-table entries

OR13C8Not classified

Variant type: missense_variant
Chromosome / position: 9:107331504
HGVS: NM_001004483.1,c.56C>A,p.Ala19Asp
Allele change: Missense_A19D

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.