ClinVar Miner

List of variants reported as likely pathogenic for Platelet-type bleeding disorder 10 by Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001001548.3(CD36):c.1150del (p.Ala384fs)	rs551607784	0.00157
NM_001001548.3(CD36):c.1416_*1del (p.Lys472fs)	rs771061715

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