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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLR3B
(V523E +1 more)
Single nucleotide variant
(missense variant)
not specified
+8 more
GPathogenic/Likely pathogenic
POLR3B
(P925L +1 more)
Single nucleotide variant
(missense variant)
Hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism
+1 more
GUncertain significance