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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZFP36L2
Deletion
(inframe_deletion)
Oocyte maturation defect 13
GPathogenic
RC3H1
(R688*)
Single nucleotide variant
(nonsense)
Hemophagocytic lymphohistiocytosis, familial, 6
GPathogenic