Variant (rsID / SNP)
rs569108
rs569108 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MS4A2. Location: chromosome 11, position 59,863,104. Clinical significance in the table: risk factor.
Reference-table entries
MS4A2Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:59863104
- Cytoband
- 11q12.1
- HGVS
- NM_000139.5(MS4A2):c.710A>G (p.Glu237Gly)
- Allele change
- Missense_E192G
Associated conditions / phenotypes
Atopic asthma, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.