Variant (rsID / SNP)
rs608433
rs608433 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF236. Location: chromosome 18, position 74,611,127. The table records no clinical significance for this variant.
Reference-table entries
ZNF236Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:74611127
- HGVS
- NM_001306089.2,c.1843A>G,p.Ile615Val
- Allele change
- Missense_I615V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.