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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDST, FLG
(R2447*)
Single nucleotide variant
(nonsense)
FLG-related disorders
+3 more
GPathogenic/Likely pathogenic
CCDST, FLG
(R788*)
Single nucleotide variant
(nonsense)
FLG-related condition
+2 more
GPathogenic/Likely pathogenic
CCDST, FLG
(S761fs)
Microsatellite
(frameshift variant)
FLG-related disorders
+5 more
GPathogenic/Likely pathogenic
CCDST, FLG
(R501*)
Single nucleotide variant
(nonsense)
FLG-related disorders
+6 more
GPathogenic/Likely pathogenic
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