Variant (rsID / SNP)
rs11178998
rs11178998 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPH2. Location: chromosome 12, position 72,332,715. Clinical significance in the table: Benign.
Reference-table entries
TPH2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:72332715
- Cytoband
- 12q21.1
- HGVS
- NM_173353.4(TPH2):c.-52A>G
- Allele change
- Silent
Associated conditions / phenotypes
Tryptophan 5-monooxygenase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.