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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HAVCR2
(P277L)
Single nucleotide variant
(missense variant)
not provided
GBenign
HAVCR2
Single nucleotide variant
(intron variant)
not provided
GBenign
CYFIP2, FNDC9
+8 more
Duplication
Lymphoproliferative syndrome 1
GUncertain significance
CYFIP2, FNDC9
+8 more
Deletion
Lymphoproliferative syndrome 1
GPathogenic
CYFIP2, FNDC9
+8 more
Deletion
not provided
GUncertain significance
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