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Variant (rsID / SNP)

rs12135078

OR2W3

rs12135078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2W3. Location: chromosome 1, position 248,059,456. The table records no clinical significance for this variant.

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Reference-table entries

OR2W3Not classified
Variant type
missense_variant
Chromosome / position
1:248059456
HGVS
NM_001001957.2,c.568G>A,p.Val190Ile
Allele change
Missense_V190I

Public references

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