Variant (rsID / SNP)

rs12150427

rs12150427 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR1A2. Location: chromosome 17, position 3,101,691. The table records no clinical significance for this variant.

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Reference-table entries

OR1A2Not classified

Variant type: missense_variant
Chromosome / position: 17:3101691
HGVS: NM_012352.3,c.879G>T,p.Trp293Cys
Allele change: Missense_W293C

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.