ClinVar Miner

Variants in gene NEXN with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 6
Download table as spreadsheet
HGVS dbSNP
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.4(NEXN):c.1065T>C (p.Asp355=) rs369897647
NM_144573.4(NEXN):c.156C>T (p.Asp52=) rs371431782
NM_144573.4(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.4(NEXN):c.777A>G (p.Gln259=) rs375544798
NM_144573.4(NEXN):c.864+12T>A rs188416492

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.