List of variants in gene DBH reported as likely benign by Illumina Laboratory Services, Illumina

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: 11

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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.*89A>G	rs45602440	0.00344
NM_000787.4(DBH):c.1085C>T (p.Ala362Val)	rs75215331	0.00236
NM_000787.4(DBH):c.*394C>T	rs533126251	0.00144
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.1572C>T (p.Asn524=)	rs200509113	0.00008
NM_000787.4(DBH):c.*844C>T	rs151115868
NM_000787.4(DBH):c.1221C>T (p.Phe407=)	rs367783759

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