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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A20
(V446M +2 more)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
SLC6A20
(L278fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance