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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126860890, MKX
(L223F)
Single nucleotide variant
(missense variant)
MKX-related disorder
GUncertain significance
LOC126860890, MKX
Single nucleotide variant
(synonymous variant)
MKX-related disorder
GLikely benign