"Division of Medical Genetics, University of Washington"[submitter] AN - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 412519	NM_020937.4(FANCM):c.5101C>T (p.Gln1701Ter)	FANCM (Q1701* +1 more)	Single nucleotide variant (nonsense)	Premature ovarian failure 15 +5 more	GConflicting classifications of pathogenicity
Select item 526381	NM_020937.4(FANCM):c.5791C>T (p.Arg1931Ter)	FANCM (R1931* +1 more)	Single nucleotide variant (nonsense)	Spermatogenic failure 28 +6 more	GConflicting classifications of pathogenicity