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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LYST
(Y2278C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
LYST
(V1678A)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome
+1 more
GUncertain significance
LYST
(V773M)
Single nucleotide variant
(missense variant)
Chédiak-Higashi syndrome
GUncertain significance
LYST
(K589R)
Single nucleotide variant
(missense variant)
Chédiak-Higashi syndrome
GUncertain significance
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