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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EHHADH
(S301fs +1 more)
Duplication
(frameshift variant)
Fanconi renotubular syndrome 3
GLikely benign
EHHADH
(G101E +1 more)
Single nucleotide variant
(missense variant)
not specified
GBenign