Variant (rsID / SNP)
rs1063639
rs1063639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HDAC4. Location: chromosome 2, position 240,003,870. The table records no clinical significance for this variant.
Reference-table entries
HDAC4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:240003870
- HGVS
- NM_001378414.1,c.2580C>T,p.Pro860Pro
- Allele change
- Synonymous_P855P
Associated conditions / phenotypes
Schizophrenia|Obsessive-Compulsive Disorder|Thyroid Carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.