List of variants in gene NSD2 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001042424.3(NSD2):c.*1922dup	rs886059331	0.00006
NM_001042424.3(NSD2):c.1902C>T (p.Asp634=)	rs746926553	0.00004
NM_001042424.3(NSD2):c.*1370dup	rs886059325
NM_001042424.3(NSD2):c.*2012dup	rs766138833
NM_001042424.3(NSD2):c.-29-6901dup	rs886059308
NM_001042424.3(NSD2):c.3019A>C (p.Thr1007Pro)	rs2108971216

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