Variant (rsID / SNP)
rs2529541
rs2529541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAGEB2. The table records no clinical significance for this variant.
Reference-table entries
MAGEB2Not classified
- Variant type
- missense_variant
- HGVS
- NM_002364.5,c.181G>A,p.Glu61Lys
- Allele change
- Missense_E61K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
