List of variants in gene DPP6 reported as uncertain significance for heart conduction disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_130797.4(DPP6):c.1154T>C (p.Met385Thr)	rs369128533	0.00002
NM_130797.4(DPP6):c.1091C>G (p.Pro364Arg)	rs756673341

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