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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLFN14
(R587C)
Single nucleotide variant
(missense variant)
Platelet-type bleeding disorder 20
+1 more
GUncertain significance
SLFN14
(R486*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GConflicting classifications of pathogenicity
SLFN14
(R338W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLFN14
(M331I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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