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Variant (rsID / SNP)

rs17128086

OR10G6

rs17128086 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10G6. Location: chromosome 11, position 123,864,948. The table records no clinical significance for this variant.

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Reference-table entries

OR10G6Not classified
Variant type
synonymous_variant
Chromosome / position
11:123864948
HGVS
NM_001355219.1,c.921C>T,p.Ile307Ile
Allele change
Synonymous_I307I

Public references

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