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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RNF168
(L199S)
Single nucleotide variant
(missense variant)
RIDDLE syndrome
+2 more
GUncertain significance
RNF168
Microsatellite
(splice acceptor variant)
RIDDLE syndrome
+1 more
GLikely pathogenic
RNF168
(E177K)
Single nucleotide variant
(missense variant)
RIDDLE syndrome
+1 more
GUncertain significance
RNF168
(R166G)
Single nucleotide variant
(missense variant)
RIDDLE syndrome
GUncertain significance
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