C1969060[trait identifier] AND "OMIM"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1083	NM_001080413.3(NOBOX):c.1064G>A (p.Arg355His)	NOBOX (R355H)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 167877	NM_001080413.3(NOBOX):c.1048G>T (p.Val350Leu)	NOBOX (V350L)	Single nucleotide variant (missense variant)	Premature ovarian failure 5	GPathogenic
Select item 167876	NM_001080413.3(NOBOX):c.1025G>C (p.Ser342Thr)	NOBOX (S342T)	Single nucleotide variant (missense variant)	Premature ovarian failure 5	GPathogenic
Select item 167873	NM_001080413.3(NOBOX):c.907C>T (p.Arg303Ter)	NOBOX (R303*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 167875	NM_001080413.3(NOBOX):c.349C>T (p.Arg117Trp)	NOBOX (R117W)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 167874	NM_001080413.3(NOBOX):c.271G>T (p.Gly91Trp)	NOBOX (G91W)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity

ClinVar