ClinVar Miner

List of variants studied for X-linked lymphoproliferative disease due to SH2D1A deficiency by Center for Human Genetics, Inc, Center for Human Genetics, Inc

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002351.5(SH2D1A):c.192G>A (p.Trp64Ter) rs1556620706
NM_002351.5(SH2D1A):c.385T>C (p.Ter129Arg) rs111033625
NM_002351.5(SH2D1A):c.5A>G (p.Asp2Gly) rs1556619319

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.