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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF23
(T239M)
Single nucleotide variant
(missense variant)
Autosomal dominant hypophosphatemic rickets
+3 more
GBenign
FGF23
(P195S)
Single nucleotide variant
(missense variant)
Tumoral calcinosis, hyperphosphatemic, familial, 2
+2 more
GBenign/Likely benign
FGF23
Single nucleotide variant
(intron variant)
Autosomal dominant hypophosphatemic rickets
+2 more
GBenign
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