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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DDHD2
(D376G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GLikely benign
DDHD2
(S612A +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary spastic paraplegia 54
+1 more
GUncertain significance