Related gene-specific medical variations for Gene (Select 140870) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3089806	NM_001198986.2(EPPIN-WFDC6):c.479G>A (p.Cys160Tyr)	EPPIN-WFDC6, WFDC6 (C160Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089805	NM_001198986.2(EPPIN-WFDC6):c.469A>G (p.Asn157Asp)	EPPIN-WFDC6, WFDC6 (N57D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089804	NM_001198986.2(EPPIN-WFDC6):c.457G>T (p.Asp153Tyr)	EPPIN-WFDC6, WFDC6 (D153Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089803	NM_001198986.2(EPPIN-WFDC6):c.434T>C (p.Ile145Thr)	EPPIN-WFDC6, WFDC6 (I145T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089802	NM_001198986.2(EPPIN-WFDC6):c.400C>T (p.Pro134Ser)	EPPIN-WFDC6, WFDC6 (P134S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089801	NM_001198986.2(EPPIN-WFDC6):c.395C>T (p.Pro132Leu)	EPPIN-WFDC6, WFDC6 (P32L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2218934	NM_080827.2(WFDC6):c.121G>A (p.Glu41Lys)	EPPIN-WFDC6, WFDC6 (E41K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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