Related gene-specific medical variations for Gene (Select 23286) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3190864	NM_015238.3(WWC1):c.889C>A (p.Gln297Lys)	LOC126807584, WWC1 (Q297K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190862	NM_015238.3(WWC1):c.47G>A (p.Arg16His)	LOC129995211, WWC1 (R16H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656035	NM_015238.3(WWC1):c.-5G>A	LOC129995211, WWC1	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 2656034	NM_015238.3(WWC1):c.-6G>A	LOC129995211, WWC1	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 2534742	NM_015238.3(WWC1):c.86A>G (p.Asn29Ser)	LOC129995211, WWC1 (N29S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2387325	NM_015238.3(WWC1):c.20C>G (p.Pro7Arg)	LOC129995211, WWC1 (P7R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267984	NM_015238.3(WWC1):c.107A>G (p.Asp36Gly)	LOC129995211, WWC1 (D36G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 91990	NM_015238.3(WWC1):c.1906G>A (p.Ala636Thr)	WWC1 (A636T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar