Variant (rsID / SNP)
rs10013040
rs10013040 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEIL3. Location: chromosome 4, position 178,231,152. The table records no clinical significance for this variant.
Reference-table entries
NEIL3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:178231152
- HGVS
- NM_018248.3,c.45C>A,p.Arg15Arg
- Allele change
- Synonymous_R15R
Associated conditions / phenotypes
Myocardial Infarction
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.