Variant (rsID / SNP)
rs57919558
rs57919558 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH24. Location: chromosome 14, position 23,520,641. The table records no clinical significance for this variant.
Reference-table entries
CDH24Not classified
- Variant type
- intron_variant
- Chromosome / position
- 14:23520641
- HGVS
- NM_022478.4,c.1477+538T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.