ClinVar Miner

List of variants reported as benign for Beckwith-Wiedemann syndrome by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (7):

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_001122630.2(CDKN1C):c.567A>G (p.Pro189=)	rs529326848	0.03671
NM_001122630.2(CDKN1C):c.702G>A (p.Gly234=)	rs556682082	0.00065
NM_001122630.2(CDKN1C):c.573GGCCCC[3] (p.186AP[9])	rs759134767

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