Variant (rsID / SNP)
rs138650483
rs138650483 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MS4A6A. Location: chromosome 11, position 59,940,500. The table records no clinical significance for this variant.
Reference-table entries
MS4A6ANot classified
- Variant type
- splice_donor_variant&intron_variant
- Chromosome / position
- 11:59940500
- HGVS
- NM_001330275.1,c.735+1G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.