List of variants in gene combination ITGA2, MOCS2 reported as likely benign for Platelet-type bleeding disorder 9

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

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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

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