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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC34A1
(R25Q)
Single nucleotide variant
(missense variant)
Hypophosphatemic nephrolithiasis/osteoporosis 1
+1 more
GConflicting classifications of pathogenicity
SLC34A1
Deletion
(inframe_deletion)
not provided
+3 more
GConflicting classifications of pathogenicity
SLC34A1
Single nucleotide variant
(splice acceptor variant)
not provided
GLikely pathogenic
F12, SLC34A1
(T328K)
Single nucleotide variant
(missense variant)
Hereditary angioneurotic edema
+3 more
GPathogenic
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