Variant (rsID / SNP)
rs2530223
rs2530223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HDAC3. Location: chromosome 5, position 141,014,494. The table records no clinical significance for this variant.
Reference-table entries
HDAC3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 5:141014494
- HGVS
- NM_001355039.2,c.165A>G,p.Gln55Gln
- Allele change
- Silent
Associated conditions / phenotypes
Schizophrenia|Type 2 Diabetes Mellitus|Diabetes Mellitus|Migraine with or Without Aura 1|Headache
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.