Variant (rsID / SNP)

rs2874103

rs2874103 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR4E2. Location: chromosome 14, position 22,133,648. The table records no clinical significance for this variant.

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Reference-table entries

OR4E2Not classified

Variant type: missense_variant
Chromosome / position: 14:22133648
HGVS: NM_001001912.3,c.352G>A,p.Val118Met
Allele change: Missense_V118M

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.