Variant (rsID / SNP)
rs4613440
rs4613440 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRIP2. Location: chromosome 3, position 14,555,811. The table records no clinical significance for this variant.
Reference-table entries
GRIP2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:14555811
- HGVS
- NM_001080423.4,c.1479T>C,p.Ser493Ser
- Allele change
- Missense_V494A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.