Variant (rsID / SNP)

rs7305115

rs7305115 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPH2. Location: chromosome 12, position 72,372,862. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TPH2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:72372862
Cytoband: 12q21.1
HGVS: NM_173353.4(TPH2):c.936A>G (p.Pro312=)
Allele change: Synonymous_P312P

Associated conditions / phenotypes

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.