Variant (rsID / SNP)
rs527025
rs527025 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZSCAN5B. Location: chromosome 19, position 56,703,248. The table records no clinical significance for this variant.
Reference-table entries
ZSCAN5BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 19:56703248
- HGVS
- NM_001080456.5,c.559C>T,p.Pro187Ser
- Allele change
- Missense_P187S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
