Related gene-specific medical variations for Gene (Select 164237) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3190471	NM_172005.2(WFDC13):c.82G>A (p.Val28Ile)	WFDC10B, WFDC13 (V28I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190470	NM_172005.2(WFDC13):c.79C>T (p.Arg27Cys)	WFDC10B, WFDC13 (R27C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190469	NM_172005.2(WFDC13):c.205G>A (p.Val69Ile)	WFDC10B, WFDC13 (V69I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3190468	NM_172006.2(WFDC10B):c.-178G>A	WFDC10B, WFDC13 (S9N)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2541420	NM_172006.2(WFDC10B):c.-133G>A	WFDC10B, WFDC13 (C24Y)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2303887	NM_172005.2(WFDC13):c.95T>A (p.Ile32Asn)	WFDC10B, WFDC13 (I32N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226905	NM_172005.2(WFDC13):c.14T>G (p.Leu5Arg)	WFDC10B, WFDC13 (L5R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 780608	NM_172005.2(WFDC13):c.111C>T (p.Pro37=)	WFDC10B, WFDC13	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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