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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRPPRC
(E674K)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
LRPPRC
(I560L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
LRPPRC
(T476A)
Single nucleotide variant
(missense variant)
LRPPRC-related disorder
+2 more
GConflicting classifications of pathogenicity
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