Variant (rsID / SNP)
rs6591561
rs6591561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MS4A4A. Location: chromosome 11, position 60,070,176. The table records no clinical significance for this variant.
Reference-table entries
MS4A4ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 11:60070176
- HGVS
- NM_148975.3,c.532A>G,p.Met178Val
- Allele change
- Missense_M178V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.