Variant (rsID / SNP)
rs120074176
rs120074176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPH2. Location: chromosome 12, position 72,372,833. Clinical significance in the table: risk factor.
Reference-table entries
TPH2Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:72372833
- Cytoband
- 12q21.1
- HGVS
- NM_173353.4(TPH2):c.907C>T (p.Arg303Trp)
- Allele change
- Missense_R303W
Associated conditions / phenotypes
Attention deficit-hyperactivity disorder, susceptibility to, 7
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.