ClinVar Miner

List of variants in gene CD40LG reported as benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP
NM_000074.2(CD40LG):c.148T>C (p.Leu50=) rs1126535
NM_000074.2(CD40LG):c.38C>T (p.Ala13Val) rs368003929
NM_000074.2(CD40LG):c.410-13T>C rs3092923
NM_000074.2(CD40LG):c.542G>A (p.Arg181Gln) rs11575982
NM_000074.2(CD40LG):c.542G>C (p.Arg181Pro) rs11575982
NM_000074.2(CD40LG):c.655G>A (p.Gly219Arg) rs148594123
NM_000074.2(CD40LG):c.684A>G (p.Val228=) rs11575983
NM_000074.2(CD40LG):c.81A>G (p.Leu27=) rs36063307
NM_000074.3(CD40LG):c.32G>A (p.Arg11Gln) rs145115086
NM_000074.3(CD40LG):c.487G>A (p.Val163Ile) rs199914973
NM_000074.3(CD40LG):c.550T>A (p.Ser184Thr) rs147340102
NM_000074.3(CD40LG):c.595G>A (p.Gly199Ser) rs769728462
NM_000074.3(CD40LG):c.601T>C (p.Phe201Leu) rs144827029

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.