List of variants in gene NSD1 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: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022455.5(NSD1):c.4605C>T (p.Arg1535=)	rs140229717	0.00010
NM_022455.5(NSD1):c.*1014dup	rs886060448	0.00005
NM_022455.5(NSD1):c.*4596del	rs886060459	0.00003
NM_022455.5(NSD1):c.1063+10dup	rs762416925	0.00001
NM_022455.5(NSD1):c.*216CCAA[1]	rs886060444
NM_022455.5(NSD1):c.4609_4611del	rs60995782
NM_022455.5(NSD1):c.4610_4611del	rs60995782
NM_022455.5(NSD1):c.4610_4611dup	rs60995782
NM_022455.5(NSD1):c.*4611dup	rs60995782
NM_022455.5(NSD1):c.*4612del	rs886060465
NM_022455.5(NSD1):c.*565del	rs886060446
NM_022455.5(NSD1):c.*839dup	rs886060447

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.