List of variants reported as likely pathogenic for Platelet-type bleeding disorder 10 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001001548.3(CD36):c.1079T>G (p.Leu360Ter)	rs56381858	0.00017
NM_001001548.3(CD36):c.610-2A>G	rs745604189	0.00001
NM_001001548.3(CD36):c.1126-1G>A
NM_001001548.3(CD36):c.971C>G (p.Ser324Ter)	rs751804837

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