Variant (rsID / SNP)
rs60994383
rs60994383 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR4D2. Location: chromosome 17, position 56,247,101. The table records no clinical significance for this variant.
Reference-table entries
OR4D2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:56247101
- HGVS
- NM_001004707.4,c.85C>A,p.Leu29Ile
- Allele change
- Missense_L29I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.