List of variants in gene PRDM16 reported as uncertain significance for Wolff-Parkinson-White syndrome

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022114.4(PRDM16):c.2666C>T (p.Pro889Leu)	rs201814961	0.00025
NM_022114.4(PRDM16):c.706G>A (p.Asp236Asn)	rs185041492	0.00008
NM_022114.4(PRDM16):c.1642C>A (p.Pro548Thr)	rs866090726
NM_022114.4(PRDM16):c.2855C>T (p.Thr952Met)	rs749180764

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