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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM3
Single nucleotide variant
(intron variant)
not provided
GLikely benign
DNM3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
DNM3
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
ANKRD45, C1orf105
+22 more
Duplication
not provided
GUncertain significance
ANKRD45, C1orf105
+22 more
Duplication
Autoimmune lymphoproliferative syndrome type 1
GUncertain significance
GAS5, KLHL20
+22 more
Deletion
Autoimmune lymphoproliferative syndrome type 1
GPathogenic
ARL8A, CNIH4
+956 more
Duplication
Gastrointestinal stromal tumor
+2 more
GUncertain significance
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