List of variants in gene DRD3 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000796.6(DRD3):c.129C>T (p.Ile43=)	rs143953030	0.00068
NM_000796.6(DRD3):c.1047T>C (p.His349=)	rs139341493	0.00056
NM_000796.6(DRD3):c.405C>T (p.Pro135=)	rs199529083	0.00005
NM_000796.6(DRD3):c.117C>T (p.Leu39=)	rs149122773
NM_000796.6(DRD3):c.155T>C (p.Met52Thr)

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