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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPM1
(P129T)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
DPM1
(G111fs)
Deletion
(frameshift variant +1 more)
Congenital disorder of glycosylation type 1E
+2 more
GPathogenic
DPM1
(Q77E)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
DPM1, LOC130066166
(S7N)
Single nucleotide variant
(missense variant +1 more)
Congenital disorder of glycosylation type 1E
+2 more
GUncertain significance
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