List of variants in gene TACR3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001059.3(TACR3):c.579C>T (p.Pro193=)	rs62340657	0.00164
NM_001059.3(TACR3):c.12C>T (p.Leu4=)
NM_001059.3(TACR3):c.594A>T (p.Thr198=)
NM_001059.3(TACR3):c.969A>T (p.Ala323=)

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