Variant (rsID / SNP)

rs17110563

rs17110563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPH2. Location: chromosome 12, position 72,366,306. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TPH2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 12:72366306
Cytoband: 12q21.1
HGVS: NM_173353.4(TPH2):c.616C>T (p.Pro206Ser)
Allele change: Missense_P206S

Associated conditions / phenotypes

Bipolar affective disorder, susceptibility to|Tryptophan 5-monooxygenase deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.