List of variants reported as likely pathogenic for anemia by Knight Diagnostic Laboratories, Oregon Health and Sciences University

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000298.6(PKLR):c.1456C>T (p.Arg486Trp)	rs116100695	0.00270
NM_020207.7(ERCC6L2):c.19C>T (p.Gln7Ter)	rs778926161	0.00031
NM_001374504.1(TMPRSS6):c.1534G>A (p.Asp512Asn)	rs137853120	0.00006
NM_025215.6(PUS1):c.717C>A (p.Tyr239Ter)	rs779651314	0.00001
NM_004629.2(FANCG):c.1158dup (p.Ser387fs)	rs757418016
Single allele

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