Variant (rsID / SNP)
rs4947710
rs4947710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRB10. Location: chromosome 7, position 50,673,029. The table records no clinical significance for this variant.
Reference-table entries
GRB10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:50673029
- HGVS
- NM_001371009.1,c.1494A>G,p.Ala498Ala
- Allele change
- Synonymous_A443A
Associated conditions / phenotypes
Synonymous_A487A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.