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Variant (rsID / SNP)

rs1123991

OR51E2

rs1123991 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR51E2. Location: chromosome 11, position 4,703,165. The table records no clinical significance for this variant.

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Reference-table entries

OR51E2Not classified
Variant type
synonymous_variant
Chromosome / position
11:4703165
HGVS
NM_030774.4,c.777G>T,p.Val259Val
Allele change
Synonymous_V259V

Public references

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