Variant (rsID / SNP)
rs1453542
rs1453542 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR4D6. Location: chromosome 11, position 59,224,885. The table records no clinical significance for this variant.
Reference-table entries
OR4D6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:59224885
- HGVS
- NM_001004708.1,c.452G>C,p.Ser151Thr
- Allele change
- Missense_S151T
Associated conditions / phenotypes
Neutropenia|Thrombocytopenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.