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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP27B1
(R453H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CYP27B1
(P353A)
Single nucleotide variant
(missense variant)
CYP27B1-related condition
+3 more
GConflicting classifications of pathogenicity
CYP27B1
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
CYP27B1
(A129T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
CYP27B1
Single nucleotide variant
(intron variant)
CYP27B1-related condition
+1 more
GLikely benign
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