ClinVar Miner

List of variants in gene NSD1 reported as likely benign by Center for Human Genetics, Inc,Center for Human Genetics, Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
NM_022455.4(NSD1):c.1574G>A (p.Arg525Gln) rs138405802
NM_022455.4(NSD1):c.4498-10del rs200890017
NM_022455.4(NSD1):c.4765+18C>T rs751340849
NM_022455.4(NSD1):c.4966+15T>C rs587784130
NM_022455.4(NSD1):c.7850T>C (p.Leu2617Ser) rs77618751

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.