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Variant (rsID / SNP)

rs12790125

OR4C15

rs12790125 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR4C15. Location: chromosome 11, position 55,322,539. The table records no clinical significance for this variant.

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Reference-table entries

OR4C15Not classified
Variant type
missense_variant
Chromosome / position
11:55322539
HGVS
NM_001001920.3,c.595G>A,p.Val199Ile
Allele change
Missense_V253I

Public references

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