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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPM1, LOC130066166
Single nucleotide variant
(synonymous variant +1 more)
DPM1-related disorder
+1 more
GLikely benign
DPM1, LOC130066166
(R8C)
Single nucleotide variant
(missense variant +1 more)
Congenital disorder of glycosylation type 1E
+2 more
GConflicting classifications of pathogenicity