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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT17
Single nucleotide variant
(intron variant)
Steatocystoma multiplex
+2 more
GBenign/Likely benign
KRT17
(S97del)
Microsatellite
(inframe_deletion)
Steatocystoma multiplex
+2 more
GPathogenic/Likely pathogenic
KRT17
(R94H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
KRT17
(N92S)
Single nucleotide variant
(missense variant)
Abnormality of the skin
+3 more
GPathogenic
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