List of variants reported as likely pathogenic for Platelet-type bleeding disorder 10 by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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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.107del (p.Lys36fs)	rs754478799
NM_001001548.3(CD36):c.1206_1230dup (p.Val411fs)
NM_001001548.3(CD36):c.588del (p.Thr197fs)

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