C1835826[trait identifier] AND "Lupski Lab, Baylor-Hopkins CMG, Baylor - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 224359	NM_015375.3(DSTYK):c.2368C>T (p.Arg790Cys)	DSTYK (R790C)	Single nucleotide variant (missense variant)	Congenital anomalies of kidney and urinary tract 1	GUncertain significance
Select item 224360	NM_015375.3(DSTYK):c.1819-3C>T	DSTYK	Single nucleotide variant (intron variant)	Congenital anomalies of kidney and urinary tract 1 +1 more	GConflicting classifications of pathogenicity
Select item 224356	NM_015375.3(DSTYK):c.1775G>A (p.Arg592Gln)	DSTYK (R592Q)	Single nucleotide variant (missense variant)	DSTYK-related condition +2 more	GConflicting classifications of pathogenicity
Select item 224361	NM_015375.3(DSTYK):c.1253A>G (p.Asp418Gly)	DSTYK (D418G)	Single nucleotide variant (missense variant)	Congenital anomalies of kidney and urinary tract 1	GUncertain significance
Select item 224357	NM_015375.3(DSTYK):c.358G>A (p.Asp120Asn)	DSTYK (D120N)	Single nucleotide variant (missense variant)	Congenital anomalies of kidney and urinary tract 1	GUncertain significance
Select item 224358	NM_015375.3(DSTYK):c.53C>T (p.Pro18Leu)	DSTYK (P18L)	Single nucleotide variant (missense variant)	DSTYK-related condition +2 more	GConflicting classifications of pathogenicity

ClinVar