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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALDH3A2
(P114L)
Single nucleotide variant
(missense variant +1 more)
Sjögren-Larsson syndrome
GLikely pathogenic
ALDH3A2
(T184M)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
ALDH3A2
(C214fs +1 more)
Deletion
(frameshift variant)
Sjögren-Larsson syndrome
GPathogenic
ALDH3A2
(W259* +1 more)
Single nucleotide variant
(nonsense)
Sjögren-Larsson syndrome
GLikely pathogenic
ALDH3A2
(S203fs +1 more)
Microsatellite
(frameshift variant)
not provided
+1 more
GPathogenic
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