List of variants reported as likely pathogenic for hematologic disorder by Reproductive Health Research and Development, BGI Genomics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001001548.3(CD36):c.429+2T>C	rs3211893	0.00220
NM_001001548.3(CD36):c.1228_1239del (p.Ile410_Ile413del)	rs550565800
NM_005476.7(GNE):c.2086G>A (p.Val696Met)	rs121908627

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