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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDC73
Single nucleotide variant
(5 prime UTR variant)
Hyperparathyroidism
+3 more
GConflicting classifications of pathogenicity
CDC73
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic/Likely pathogenic
CDC73
(R227fs)
Insertion
(frameshift variant)
Hyperparathyroidism 2 with jaw tumors
+2 more
GPathogenic
CDC73
(V256fs)
Deletion
(frameshift variant)
Hyperparathyroidism 2 with jaw tumors
GPathogenic
CDC73
Single nucleotide variant
(intron variant)
Parathyroid carcinoma
+2 more
GLikely benign
CDC73
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign
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