Variant (rsID / SNP)
rs227584
rs227584 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HROB. Location: chromosome 17, position 42,225,547. The table records no clinical significance for this variant.
Reference-table entries
HROBNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:42225547
- HGVS
- NM_024032.5,c.376A>C,p.Thr126Pro
- Allele change
- Missense_T126P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.