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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RNASEH2C
(R145P)
Single nucleotide variant
(missense variant)
Aicardi-Goutieres syndrome 3
GUncertain significance
RNASEH2C
(E60fs)
Duplication
(frameshift variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity