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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNPO3
(Y206C +2 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant limb-girdle muscular dystrophy type 1F
+1 more
GUncertain significance
TNPO3
(W44R)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
LOC129999289, TNPO3
(A4E)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant limb-girdle muscular dystrophy type 1F
+1 more
GUncertain significance
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