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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
XDH
(I1179T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
XDH
(N1109T)
Single nucleotide variant
(missense variant)
Xanthinuria type II
+1 more
GBenign
XDH
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign/Likely benign
XDH
Single nucleotide variant
(intron variant)
Hereditary xanthinuria type 1
+1 more
GConflicting classifications of pathogenicity
XDH
Single nucleotide variant
(synonymous variant)
XDH-related disorder
+3 more
GConflicting classifications of pathogenicity
XDH
(T623I)
Single nucleotide variant
(missense variant)
Xanthinuria type II
+1 more
GConflicting classifications of pathogenicity
XDH
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GConflicting classifications of pathogenicity
XDH
Single nucleotide variant
(synonymous variant)
Hereditary xanthinuria type 1
+1 more
GConflicting classifications of pathogenicity
XDH
(T235M)
Single nucleotide variant
(missense variant)
Xanthinuria type II
+1 more
GUncertain significance
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