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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCLRE1C
Single nucleotide variant
(synonymous variant +2 more)
not specified
+4 more
GBenign/Likely benign
DCLRE1C
Single nucleotide variant
(synonymous variant +2 more)
Histiocytic medullary reticulosis
+3 more
GBenign/Likely benign
DCLRE1C
(K428N +2 more)
Single nucleotide variant
(missense variant +1 more)
Severe combined immunodeficiency due to DCLRE1C deficiency
GBenign
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