Variant (rsID / SNP)

rs17792778

rs17792778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10G3. Location: chromosome 14, position 22,038,659. The table records no clinical significance for this variant.

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Reference-table entries

OR10G3Not classified

Variant type: missense_variant
Chromosome / position: 14:22038659
HGVS: NM_001005465.2,c.217A>G,p.Ser73Gly
Allele change: Missense_S73G

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.