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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHTKD1
(R163Q)
Single nucleotide variant
(missense variant)
2-aminoadipic 2-oxoadipic aciduria
+2 more
GUncertain significance
DHTKD1
(R455Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
DHTKD1
(G729R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
DHTKD1
(S862I)
Single nucleotide variant
(missense variant)
2-aminoadipic 2-oxoadipic aciduria
+1 more
GUncertain significance
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