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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SQSTM1
Single nucleotide variant
(5 prime UTR variant +1 more)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
GUncertain significance
SQSTM1
(K154del +1 more)
Microsatellite
(inframe_deletion)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
+2 more
GUncertain significance
SQSTM1
(Q270fs +1 more)
Deletion
(frameshift variant)
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset
+2 more
GUncertain significance
SQSTM1
Deletion
(frameshift variant)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
GLikely pathogenic
SQSTM1
(P392L +1 more)
Single nucleotide variant
(missense variant)
Paget disease of bone 3
+6 more
GConflicting classifications of pathogenicity
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