Variant (rsID / SNP)
rs4452075
rs4452075 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF527. Location: chromosome 19, position 37,879,589. The table records no clinical significance for this variant.
Reference-table entries
ZNF527Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:37879589
- HGVS
- NM_032453.2,c.638A>G,p.His213Arg
- Allele change
- Missense_H213R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.