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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NHEJ1
(N187S)
Single nucleotide variant
(missense variant +1 more)
Cernunnos-XLF deficiency
GBenign
NHEJ1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign