Variant (rsID / SNP)
rs11578
rs11578 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STX16. Location: chromosome 20, position 57,253,275. Clinical significance in the table: Benign.
Reference-table entries
STX16Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:57253275
- Cytoband
- 20q13.32
- HGVS
- NM_001001433.3(STX16):c.*1928C>T
- Allele change
- Silent
Associated conditions / phenotypes
Pseudohypoparathyroidism type 1B
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.