Variant (rsID / SNP)
rs11101192
rs11101192 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHAT. Location: chromosome 10, position 50,854,767. Clinical significance in the table: Benign.
Reference-table entries
CHATBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:50854767
- Cytoband
- 10q11.23
- HGVS
- NM_020549.5(CHAT):c.1281+47G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.