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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSG1, DSG1-AS1
(A621G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DSG1, DSG1-AS1
+1 more
(G870S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DSG1, DSG1-AS1
(G978V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
DSG1-AS1, DSG4
Single nucleotide variant
(splice donor variant)
Hypotrichosis 6
GPathogenic
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