ClinVar Miner

List of variants in gene LHB reported as pathogenic for Leydig cell hypoplasia

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_000894.2(LHB):c.167G>A (p.Gly56Asp) rs121912517
NM_000894.2(LHB):c.183+1G>C rs786204822
NM_000894.2(LHB):c.183+1G>T rs786204822
NM_000894.2(LHB):c.221A>G (p.Gln74Arg) rs5030773
NM_000894.2(LHB):c.28_39del (p.Leu10_Leu13del) rs769066903
NM_000894.2(LHB):c.88_96del (p.His30_Ile32del) rs786204823

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.