Variant (rsID / SNP)
rs998075
rs998075 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGF2R. Location: chromosome 6, position 160,468,278. The table records no clinical significance for this variant.
Reference-table entries
IGF2RNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:160468278
- HGVS
- NM_000876.4,c.2139A>G,p.Thr713Thr
- Allele change
- Synonymous_T713T
Associated conditions / phenotypes
Osteogenic Sarcoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.