"Ambry Genetics"[submitter] AND "KLK6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2481385	NM_002774.4(KLK6):c.714A>T (p.Gln238His)	KLK6 (Q238H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2210857	NM_002774.4(KLK6):c.649C>T (p.Pro217Ser)	KLK6 (P110S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2273755	NM_002774.4(KLK6):c.641G>A (p.Gly214Asp)	KLK6 (G107D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2486235	NM_002774.4(KLK6):c.590C>T (p.Ser197Phe)	KLK6 (S90F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461742	NM_002774.4(KLK6):c.380T>C (p.Leu127Pro)	KLK6 (L127P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374313	NM_002774.4(KLK6):c.346G>A (p.Ala116Thr)	KLK6 (A9T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460008	NM_002774.4(KLK6):c.271C>T (p.Arg91Trp)	KLK6 (R91W)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2381322	NM_002774.4(KLK6):c.248C>T (p.Ser83Phe)	KLK6 (P31S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign

ClinVar