ClinVar Miner

List of variants in gene ARX 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: 18
Download table as spreadsheet
HGVS dbSNP
NM_139058.3(ARX):c.1033C>A (p.Arg345=) rs1601948273
NM_139058.3(ARX):c.1269C>T (p.His423=) rs794727656
NM_139058.3(ARX):c.1448+9C>A rs759009252
NM_139058.3(ARX):c.1488C>T (p.Thr496=) rs773666007
NM_139058.3(ARX):c.1515A>G (p.Thr505=) rs398124509
NM_139058.3(ARX):c.1599C>G (p.Ala533=) rs1057523196
NM_139058.3(ARX):c.166A>G (p.Ser56Gly) rs144098296
NM_139058.3(ARX):c.264G>A (p.Leu88=) rs1556056513
NM_139058.3(ARX):c.558G>T (p.Pro186=) rs748764628
NM_139058.3(ARX):c.602C>A (p.Pro201Gln) rs1484238484
NM_139058.3(ARX):c.611G>A (p.Arg204His) rs755745002
NM_139058.3(ARX):c.642C>A (p.Ala214=) rs997439358
NM_139058.3(ARX):c.663C>G (p.Thr221=) rs1006404746
NM_139058.3(ARX):c.678C>T (p.Asp226=) rs764730866
NM_139058.3(ARX):c.708T>C (p.Asp236=) rs763458576
NM_139058.3(ARX):c.807C>T (p.Ala269=) rs587783205
NM_139058.3(ARX):c.855G>A (p.Glu285=) rs139301257
NM_139058.3(ARX):c.921C>A (p.Gly307=) rs398124519

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.