Variant (rsID / SNP)
rs7124513
rs7124513 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUDT8. Location: chromosome 11, position 67,395,714. The table records no clinical significance for this variant.
Reference-table entries
NUDT8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:67395714
- HGVS
- NM_001243750.2,c.414G>A,p.Glu138Glu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
