Variant (rsID / SNP)
rs751122
rs751122 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP2B2. Location: chromosome 3, position 10,420,087. The table records no clinical significance for this variant.
Reference-table entries
ATP2B2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:10420087
- HGVS
- NM_001001331.4,c.1050A>G,p.Gln350Gln
- Allele change
- Synonymous_Q305Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.