ClinVar for PubMed (Select 20887964) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1805596	NM_018117.12(WDR11):c.3665T>C (p.Ile1222Thr)	WDR11 (I1222T)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism 14 with or without anosmia +1 more	GConflicting classifications of pathogenicity
Select item 68842	NM_018117.12(WDR11):c.3450T>G (p.Phe1150Leu)	WDR11 (F1150L)	Single nucleotide variant (missense variant)	See cases +2 more	GConflicting classifications of pathogenicity
Select item 68841	NM_018117.12(WDR11):c.2932A>C (p.Lys978Gln)	WDR11 (K978Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 68840	NM_018117.12(WDR11):c.2070T>A (p.His690Gln)	WDR11 (H690Q)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism 14 with anosmia	GPathogenic
Select item 68839	NM_018117.12(WDR11):c.1343G>A (p.Arg448Gln)	WDR11 (R448Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 68838	NM_018117.12(WDR11):c.1183C>T (p.Arg395Trp)	WDR11 (R395W)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 37309	NM_018117.12(WDR11):c.1303G>A (p.Ala435Thr)	WDR11 (A435T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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