ClinVar Miner

List of variants reported as likely pathogenic for Platelet-type bleeding disorder 10 by Beijing Key Laboratry for Genetics of Birth Defects, Beijing Children's Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001001548.3(CD36):c.1142T>G (p.Leu381Ter)	rs775478465	0.00001
NM_001001548.3(CD36):c.1228_1239del (p.Ile410_Ile413del)	rs550565800

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