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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLG
(K38E)
Single nucleotide variant
(missense variant)
Plasminogen deficiency, type I
+2 more
GConflicting classifications of pathogenicity
PLG
Single nucleotide variant
(intron variant)
Plasminogen deficiency, type I
GUncertain significance
PLG
(P406Q)
Single nucleotide variant
(missense variant)
Plasminogen deficiency, type I
GUncertain significance
PLG
(S760G)
Single nucleotide variant
(missense variant)
Plasminogen deficiency, type I
GUncertain significance
FNDC1, FRMD1
+86 more
Complex
Coffin-Siris syndrome 1
GPathogenic
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