ClinVar Miner

List of variants in gene NYX reported as likely benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_001378477.1(NYX):c.*152A>G
NM_022567.2(NYX):c.*414C>T rs58930096
NM_022567.2(NYX):c.*736G>C rs141612904
NM_022567.2(NYX):c.1035G>A (p.Glu345=) rs143486101
NM_022567.2(NYX):c.1198G>A (p.Gly400Ser) rs189924262
NM_022567.2(NYX):c.1227C>T (p.Thr409=) rs187149252
NM_022567.2(NYX):c.1394G>T (p.Cys465Phe) rs374968384
NM_022567.2(NYX):c.843G>A (p.Glu281=) rs3810733

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.