List of variants reported as likely pathogenic for hematologic disorder by Leiden Open Variation Database

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.3031C>T (p.Arg1011Cys)	rs142377616	0.00006
NM_000135.4(FANCA):c.1683_1689del (p.Gly562fs)	rs2039643136
NM_000135.4(FANCA):c.1A>C (p.Met1Leu)	rs772751654
NM_000135.4(FANCA):c.3240-2A>G	rs2038478110
NM_000135.4(FANCA):c.4010+1G>A	rs2062067810
NM_000135.4(FANCA):c.4285_4288dup (p.Pro1430fs)	rs2049528619
NM_004629.2(FANCG):c.1359del (p.Ala454fs)	rs1829066243
NM_006296.7(VRK2):c.102_105dup	rs759217526

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