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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATL1
(L57F)
Single nucleotide variant
(missense variant)
Neuropathy, hereditary sensory, type 1D
GUncertain significance
ATL1
(T278I)
Single nucleotide variant
(missense variant)
Neuropathy, hereditary sensory, type 1D
GUncertain significance
ATL1
(N355K)
Single nucleotide variant
(missense variant)
Osteomyelitis leading to amputation due to slow healing fractures
+3 more
GPathogenic
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