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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RECQL
(I156M)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
RECQL
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GUncertain significance
RECQL
(T29M)
Single nucleotide variant
(missense variant)
RECQL-related disorder
+4 more
GConflicting classifications of pathogenicity
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