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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SEPTIN9
Single nucleotide variant
(5 prime UTR variant +1 more)
Amyotrophic neuralgia
GPathogenic
SEPTIN9
(R88W +3 more)
Single nucleotide variant
(missense variant +1 more)
Amyotrophic neuralgia
+1 more
GPathogenic
SEPTIN9
(S93F +3 more)
Single nucleotide variant
(missense variant +1 more)
Amyotrophic neuralgia
GPathogenic
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