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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BPTF, LOC130061496
Microsatellite
(inframe_insertion)
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
+1 more
GUncertain significance
BPTF
(M523T)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
GUncertain significance
BPTF
Single nucleotide variant
(intron variant)
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies
GUncertain significance
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