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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPB1
(S98C)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease axonal type 2F
GUncertain significance
HSPB1
(T143S)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease axonal type 2F
GUncertain significance