Variant (rsID / SNP)
rs75602167
rs75602167 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TOP3B. Location: chromosome 22, position 22,318,354. The table records no clinical significance for this variant.
Reference-table entries
TOP3BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 22:22318354
- HGVS
- NM_001282112.2,c.1145A>G,p.His382Arg
- Allele change
- Missense_H246R
Associated conditions / phenotypes
Missense_H246R|Missense_H246R|Missense_H382R|Missense_H382R|Missense_H382R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.