Related gene-specific medical variations for Gene (Select 140832) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333059	NM_080753.3(WFDC10A):c.117A>C (p.Lys39Asn)	WFDC10A, WFDC9 (K39N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190466	NM_080753.3(WFDC10A):c.119T>A (p.Val40Asp)	WFDC10A, WFDC9 (V40D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541409	NM_080753.3(WFDC10A):c.55G>T (p.Ala19Ser)	WFDC10A, WFDC9 (A19S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488285	NM_080753.3(WFDC10A):c.155A>T (p.His52Leu)	WFDC10A, WFDC9 (H52L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473916	NM_080753.3(WFDC10A):c.81G>C (p.Lys27Asn)	WFDC10A, WFDC9 (K27N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463528	NM_080753.3(WFDC10A):c.73G>A (p.Asp25Asn)	WFDC10A, WFDC9 (D25N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339922	NM_080753.3(WFDC10A):c.78G>C (p.Lys26Asn)	WFDC10A, WFDC9 (K26N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277754	NM_080753.3(WFDC10A):c.193A>G (p.Ile65Val)	WFDC10A, WFDC9 (I65V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220136	NM_080753.3(WFDC10A):c.13A>G (p.Thr5Ala)	WFDC10A, WFDC9 (T5A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2214996	NM_080753.3(WFDC10A):c.185C>A (p.Ala62Glu)	WFDC10A, WFDC9 (A62E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance