Variant (rsID / SNP)
rs7232
rs7232 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MS4A6A. Location: chromosome 11, position 59,940,599. The table records no clinical significance for this variant.
Reference-table entries
MS4A6ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 11:59940599
- HGVS
- NM_001330275.1,c.637A>T,p.Thr213Ser
- Allele change
- Missense_N150I
Associated conditions / phenotypes
Alzheimer Disease|Mild Cognitive Impairment
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.