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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLG-AS1, FLG
(R2829H)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CCDST, FLG
(S761fs)
Microsatellite
(frameshift variant)
Dermatitis, atopic, 2
+4 more
GPathogenic/Likely pathogenic
CCDST, FLG
(R501*)
Single nucleotide variant
(nonsense)
Dermatitis, atopic, 2
+5 more
GPathogenic/Likely pathogenic
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