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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FTL
(H148fs)
Duplication
(frameshift variant)
Neuroferritinopathy
Gnot provided
FTL
(H148fs)
Duplication
(frameshift variant)
Neuroferritinopathy
Gnot provided
FTL
(H153fs)
Duplication
(frameshift variant)
Neuroferritinopathy
GPathogenic
FTL
(R154fs)
Duplication
(frameshift variant)
Neuroferritinopathy
+1 more
GPathogenic
FTL
(L162fs)
Duplication
(frameshift variant)
Neuroferritinopathy
GPathogenic
FTL
Single nucleotide variant
(synonymous variant)
Hereditary hyperferritinemia with congenital cataracts
+1 more
GLikely benign
FTL
(F167fs)
Microsatellite
(frameshift variant)
Neuroferritinopathy
GPathogenic
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