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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126807125, SLC39A8
Microsatellite
(intron variant)
SLC39A8-related disorder
GLikely benign
LOC126807125, SLC39A8
Single nucleotide variant
(synonymous variant)
SLC39A8-related disorder
GLikely benign