List of variants in gene DBH reported 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
		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.76G>A (p.Val26Met)	rs76856960	0.00348
NM_000787.4(DBH):c.1085C>T (p.Ala362Val)	rs75215331	0.00236
NM_000787.4(DBH):c.933C>T (p.Tyr311=)	rs3025400	0.00217
NM_000787.4(DBH):c.1772A>T (p.Glu591Val)	rs75512464	0.00096
NM_000787.4(DBH):c.807C>T (p.Cys269=)	rs141816448	0.00050
NM_000787.4(DBH):c.1025-6T>A	rs199926239	0.00034
NM_000787.4(DBH):c.1599G>A (p.Ala533=)	rs377563744	0.00008
NM_000787.4(DBH):c.1677G>A (p.Ala559=)

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