Variant (rsID / SNP)

rs10985704

rs10985704 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR1L8, OR1J2. Location: chromosome 9, position 125,330,678. The table records no clinical significance for this variant.

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Reference-table entries

OR1L8Not classified

Variant type: missense_variant
Chromosome / position: 9:125330678
HGVS: NM_001004454.2,c.79A>C,p.Thr27Pro
Allele change: Missense_T27P

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.