Variants in gene DBH with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_000787.4(DBH):c.235C>T (p.Arg79Trp)	rs77273740	0.01166
NM_000787.4(DBH):c.747C>T (p.Tyr249=)	rs35465867	0.00428
NM_000787.4(DBH):c.263G>C (p.Gly88Ala)	rs3025380	0.00352
NM_000787.4(DBH):c.1735C>T (p.Leu579=)	rs61733931	0.00113
NM_000787.4(DBH):c.105C>T (p.Ala35=)	rs140025171	0.00026
NM_000787.4(DBH):c.850G>A (p.Asp284Asn)	rs13306301	0.00020
NM_000787.4(DBH):c.1572C>T (p.Asn524=)	rs200509113	0.00008
NM_000787.4(DBH):c.1221C>T (p.Phe407=)	rs367783759

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