List of variants in gene NSD2 reported as uncertain significance for chromosome 4 short arm deletion

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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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.4090G>A (p.Gly1364Ser)	rs548852837	0.00001
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.2675G>A (p.Arg892Lys)	rs2108958817
NM_001042424.3(NSD2):c.3271G>A (p.Glu1091Lys)	rs2108976523

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