Variant (rsID / SNP)
rs11558538
rs11558538 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HNMT. Location: chromosome 2, position 138,759,649. Clinical significance in the table: risk factor.
Reference-table entries
HNMTRisk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:138759649
- Cytoband
- 2q22.1
- HGVS
- NM_006895.3(HNMT):c.314C>T (p.Thr105Ile)
- Allele change
- Missense_T105I
Associated conditions / phenotypes
Inherited susceptibility to asthma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.