C1842090[trait identifier] AND "Rady Children's Institute for Genomic - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 692065	NM_001001548.3(CD36):c.1150del (p.Ala384fs)	CD36 (A229fs +5 more)	Deletion (frameshift variant +1 more)	Platelet-type bleeding disorder 10	GLikely pathogenic
Select item 692066	NM_001001548.3(CD36):c.1416_*1del (p.Lys472fs)	CD36 (K433fs +5 more)	Microsatellite (frameshift variant +1 more)	Platelet-type bleeding disorder 10 +1 more	GConflicting classifications of pathogenicity