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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FASLG
Single nucleotide variant
(intron variant)
Autoimmune lymphoproliferative syndrome, type 1b
+1 more
GLikely benign
FASLG
Deletion
(inframe_deletion +1 more)
Autoimmune lymphoproliferative syndrome, type 1b
GPathogenic