Variant (rsID / SNP)
rs7216493
rs7216493 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF213. Location: chromosome 17, position 78,327,358. The table records no clinical significance for this variant.
Reference-table entries
RNF213Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:78327358
- HGVS
- NM_001256071.3,c.10470G>A,p.Glu3490Glu
- Allele change
- Synonymous_E3490E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.