List of variants reported as uncertain significance for hematologic disorder by Centre for Human Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001164277.2(SLC37A4):c.139G>C (p.Asp47His)	rs1943672924
NM_001164277.2(SLC37A4):c.152TCA[1] (p.Ile52del)	rs1943642881

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