ClinVar Miner

List of variants reported as likely pathogenic for Emery-Dreifuss muscular dystrophy 4, autosomal dominant

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_182961.4(SYNE1):c.4499T>A (p.Ile1500Asn) rs746438011 0.00001
NC_000006.11:g.(152861157_152949399)_(152949690_152957772)del
NM_182961.4(SYNE1):c.18382-1G>A rs762660111
NM_182961.4(SYNE1):c.19260+2T>C rs1588855714
NM_182961.4(SYNE1):c.19672C>T (p.Gln6558Ter) rs2086610889
NM_182961.4(SYNE1):c.2624del (p.Gly875fs)
NM_182961.4(SYNE1):c.3175A>T (p.Lys1059Ter)

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.