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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLOD3
(S483L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
PLOD3
(I461L)
Single nucleotide variant
(missense variant)
Bone fragility with contractures, arterial rupture, and deafness
GUncertain significance
PLOD3
(D326N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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