List of variants in gene TPH2 reported as uncertain significance for inherited disease susceptibility

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_173353.4(TPH2):c.616C>T (p.Pro206Ser)	rs17110563	0.00107
NM_173353.4(TPH2):c.710G>A (p.Arg237Gln)
NM_173353.4(TPH2):c.983C>G (p.Ala328Gly)	rs2887147

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