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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRDX5, TRMT112
(L17I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
PRDX5, TRMT112
(G19R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign