List of variants reported as uncertain significance for hematologic disorder by Myriad Genetics, Inc.

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.809A>T (p.Lys270Ile)	rs121965070	0.00055
NM_000135.4(FANCA):c.4199G>A (p.Arg1400His)	rs149851163	0.00003
NM_015506.3(MMACHC):c.800G>A (p.Arg267Gln)	rs765822392	0.00002
NM_000128.4(F11):c.365G>A (p.Gly122Asp)	rs369650561	0.00001
NM_000135.4(FANCA):c.3382C>G (p.Gln1128Glu)	rs1439817346	0.00001
NM_152564.5(VPS13B):c.5220G>T (p.Glu1740Asp)	rs780598553	0.00001
NM_000135.4(FANCA):c.2778+83C>G	rs750997715
NM_152564.5(VPS13B):c.11673_11674del (p.Ala3892fs)	rs1180933570

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