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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RXYLT1
(K6R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
RXYLT1
(E52G)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance