List of variants reported as pathogenic for hematologic disorder by University of Washington Center for Mendelian Genomics, University of Washington

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001029.5(RPS26):c.259C>T (p.Arg87Ter)	rs148942765
NM_001029.5(RPS26):c.4-2A>T	rs786203998
NM_001031.5(RPS28):c.1A>G (p.Met1Val)	rs786203997
NM_006019.4(TCIRG1):c.2206C>A (p.Arg736Ser)	rs587779413
NM_007294.4(BRCA1):c.5095C>T (p.Arg1699Trp)	rs55770810
NM_007294.4(BRCA1):c.594_597delTGTG	rs797045175
NM_058163.3(TSR2):c.191A>G (p.Glu64Gly)	rs786203996

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