Variant (rsID / SNP)
rs12648093
rs12648093 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUDT6. Location: chromosome 4, position 123,838,758. The table records no clinical significance for this variant.
Reference-table entries
NUDT6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:123838758
- HGVS
- NM_007083.5,c.340T>C,p.Cys114Arg
- Allele change
- Missense_C114R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.