"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 790908	NM_000379.4(XDH):c.3536T>C (p.Ile1179Thr)	XDH (I1179T)	Single nucleotide variant (missense variant)	Xanthinuria type II +3 more	GConflicting classifications of pathogenicity
Select item 896915	NM_000379.4(XDH):c.3326A>C (p.Asn1109Thr)	XDH (N1109T)	Single nucleotide variant (missense variant)	Xanthinuria type II +1 more	GBenign
Select item 335770	NM_000379.4(XDH):c.2634T>C (p.Ile878=)	XDH	Single nucleotide variant (synonymous variant)	Xanthinuria type II +3 more	GConflicting classifications of pathogenicity
Select item 790933	NM_000379.4(XDH):c.1868C>T (p.Thr623Ile)	XDH (T623I)	Single nucleotide variant (missense variant)	Xanthinuria type II +1 more	GConflicting classifications of pathogenicity
Select item 786264	NM_000379.4(XDH):c.882C>T (p.Pro294=)	XDH	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 715344	NM_000379.4(XDH):c.822G>A (p.Leu274=)	XDH	Single nucleotide variant (synonymous variant)	Hereditary xanthinuria type 1 +1 more	GConflicting classifications of pathogenicity
Select item 1025638	NM_000379.4(XDH):c.704C>T (p.Thr235Met)	XDH (T235M)	Single nucleotide variant (missense variant)	Xanthinuria type II +1 more	GUncertain significance

ClinVar