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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129931894, SLC19A2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC129931894, SLC19A2
(L19P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance