List of variants in gene combination ITGA2, MOCS2 reported as likely benign for obsolete bleeding diathesis due to a collagen receptor defect

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004531.5(MOCS2):c.*321A>G	rs73756618	0.00849
NM_004531.5(MOCS2):c.*171G>C	rs191465075	0.00003
NM_002203.4(ITGA2):c.*1764del	rs3212655
NM_002203.4(ITGA2):c.*2570C>A	rs1900182
NM_004531.5(MOCS2):c.*44A>C	rs367775935

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.