Variant (rsID / SNP)
rs7515284
rs7515284 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NSUN4. Location: chromosome 1, position 46,809,419. The table records no clinical significance for this variant.
Reference-table entries
NSUN4Not classified
- Variant type
- intron_variant
- Chromosome / position
- 1:46809419
- HGVS
- NM_199044.4,c.94-1054A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.