ClinVar Miner

List of variants in gene BRWD3 reported as pathogenic for X-linked disease

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_153252.5(BRWD3):c.3198_3199TG[1] (p.Val1067fs)
NM_153252.5(BRWD3):c.3325+1G>T rs730882185
NM_153252.5(BRWD3):c.4786A>G (p.Lys1596Glu) rs137853272
NM_153252.5(BRWD3):c.568C>T (p.Arg190Ter) rs1057518650
NM_153252.5(BRWD3):c.946dup (p.Arg316fs) rs730882186

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.