Variant (rsID / SNP)
rs12453
rs12453 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MS4A6A. Location: chromosome 11, position 59,945,745. The table records no clinical significance for this variant.
Reference-table entries
MS4A6ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:59945745
- HGVS
- NM_001330275.1,c.411A>G,p.Leu137Leu
- Allele change
- Synonymous_L109L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.