List of variants in gene NSD1 reported as likely benign for Beckwith-Wiedemann 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_022455.5(NSD1):c.1797C>T (p.Ile599=)	rs1554189107
NM_022455.5(NSD1):c.2148T>G (p.Thr716=)	rs780294858
NM_022455.5(NSD1):c.7914C>T (p.Pro2638=)	rs781650846

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