ClinVar Miner

List of variants reported as uncertain significance for disorder of catecholamine synthesis by Revvity Omics, Revvity

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001082971.2(DDC):c.272C>T (p.Ala91Val)	rs137853211	0.00004
NM_001082971.2(DDC):c.206C>T (p.Thr69Met)	rs777956037	0.00002
NM_000787.4(DBH):c.259T>C (p.Phe87Leu)	rs761327487	0.00001

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