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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRP2
(E3763V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
LRP2
(I3389V)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
LRP2
(T2086S)
Single nucleotide variant
(missense variant)
Donnai-Barrow syndrome
+3 more
GBenign/Likely benign
LRP2
(S1707F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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