Variant (rsID / SNP)
rs210280
rs210280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF33B. Location: chromosome 10, position 43,089,965. The table records no clinical significance for this variant.
Reference-table entries
ZNF33BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:43089965
- HGVS
- NM_001305033.2,c.454C>T,p.Arg152Cys
- Allele change
- Silent
Associated conditions / phenotypes
Missense_R33C|Missense_R33C|Missense_R145C|Missense_R33C|Missense_R33C
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.