List of variants reported as likely benign for hematologic disorder by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_181507.2(HPS5):c.345G>A (p.Met115Ile)	rs149229493	0.00309
NM_000132.4(F8):c.396A>C (p.Glu132Asp)	rs137852388	0.00018
NM_005236.3(ERCC4):c.2545C>G (p.Gln849Glu)	rs374186605	0.00008
NM_001018113.3(FANCB):c.1216C>T (p.Arg406Trp)	rs1364046604

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