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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLFN14
(P718fs)
Deletion
(frameshift variant)
Platelet-type bleeding disorder 20
GUncertain significance
SLFN14
(L716F)
Single nucleotide variant
(missense variant)
Platelet-type bleeding disorder 20
GUncertain significance
SLFN14
(T635I)
Single nucleotide variant
(missense variant)
Platelet-type bleeding disorder 20
GUncertain significance
SLFN14
(F614L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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