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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM1, LOC113839516
(I120V)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 31
+1 more
GUncertain significance
DNM1
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
DNM1
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
DNM1
(S847L)
Single nucleotide variant
(3 prime UTR variant +1 more)
Developmental and epileptic encephalopathy, 31
+1 more
GBenign/Likely benign
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