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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HPN
(R8Q)
Single nucleotide variant
(missense variant)
not provided
GBenign
HPN, HPN-AS1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
HPN, HPN-AS1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
ALKBH6, APLP1
+83 more
Duplication
Hereditary spastic paraplegia 75
GUncertain significance
ALKBH6, APLP1
+54 more
Deletion
Brugada syndrome 5
GUncertain significance
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