List of variants reported as uncertain significance for hematologic disorder by Institute of Human Genetics, University Hospital of Duesseldorf

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.5606C>T (p.Thr1869Met)	rs117148013	0.00078
NM_152564.5(VPS13B):c.6416A>G (p.Asn2139Ser)	rs142248228	0.00070
NM_001258392.3(CLPB):c.1570C>T (p.Arg524Trp)	rs200299650	0.00005
NM_152564.5(VPS13B):c.8126G>A (p.Cys2709Tyr)

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