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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED25
Single nucleotide variant
(intron variant)
not specified
+4 more
GConflicting classifications of pathogenicity
MED25
Single nucleotide variant
(synonymous variant)
Charcot-Marie-Tooth disease
+3 more
GBenign
MED25
Single nucleotide variant
(synonymous variant)
Charcot-Marie-Tooth disease type 2
+3 more
GConflicting classifications of pathogenicity
MED25
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease type 2
+5 more
GConflicting classifications of pathogenicity
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