Variant (rsID / SNP)
rs755017
rs755017 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZBTB46. Location: chromosome 20, position 62,421,622. Clinical significance in the table: association.
Reference-table entries
ZBTB46Association
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:62421622
- Cytoband
- 20q13.33
- HGVS
- NM_001369741.1(ZBTB46):c.489T>C (p.Ala163=)
- Allele change
- Synonymous_A163A
Associated conditions / phenotypes
Chronic osteomyelitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.