List of variants in gene DBH reported by GeneReviews

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000787.3(DBH):c.-979T>C	rs1611115	0.79837
NM_000787.4(DBH):c.339+2T>C	rs74853476	0.00106
NM_000787.4(DBH):c.1033G>A (p.Asp345Asn)	rs267606761	0.00012
NM_000787.4(DBH):c.301G>A (p.Val101Met)	rs267606760	0.00005
NM_000787.4(DBH):c.1409C>T (p.Thr470Ile)	rs770407025	0.00001
NC_000009.11:g.136496870_136496871(11_15)	rs72191426
NM_000787.4(DBH):c.1085C>A (p.Ala362Glu)	rs75215331
NM_000787.4(DBH):c.1374+24T>G	rs778042927
NM_000787.4(DBH):c.1667A>G (p.Tyr556Cys)	rs863225246
NM_000787.4(DBH):c.342C>A (p.Asp114Glu)	rs77576840
NM_000787.4(DBH):c.617del (p.Glu206fs)	rs863225244
NM_000787.4(DBH):c.806G>T (p.Cys269Phe)	rs863225245

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