Variant (rsID / SNP)

rs12139390

rs12139390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2W3. Location: chromosome 1, position 248,059,476. The table records no clinical significance for this variant.

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Reference-table entries

OR2W3Not classified

Variant type: missense_variant
Chromosome / position: 1:248059476
HGVS: NM_001001957.2,c.588A>C,p.Glu196Asp
Allele change: Missense_E196D

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.