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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDST, FLG
(S3895L)
Single nucleotide variant
(missense variant)
Dermatitis, atopic, 2
GUncertain significance
CCDST, FLG
(E2555*)
Single nucleotide variant
(nonsense)
Dermatitis, atopic, 2
GUncertain significance
CCDST, FLG
(R2447*)
Single nucleotide variant
(nonsense)
Dermatitis, atopic, 2
+3 more
GPathogenic/Likely pathogenic
CCDST, FLG
(S1559*)
Single nucleotide variant
(nonsense)
Dermatitis, atopic, 2
GLikely pathogenic
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