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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFTR, LOC111674463
Single nucleotide variant
not provided
+2 more
GConflicting classifications of pathogenicity
CFTR, LOC111674463
Single nucleotide variant
CFTR-related condition
+3 more
GConflicting classifications of pathogenicity
CFTR, LOC111674463
Single nucleotide variant
not specified
+2 more
GConflicting classifications of pathogenicity
CFTR, LOC111674463
Single nucleotide variant
not specified
+3 more
GBenign/Likely benign
LOC111674463, CFTR
Single nucleotide variant
not provided
+1 more
GConflicting classifications of pathogenicity
CFTR, LOC111674463
Single nucleotide variant
not provided
+1 more
GUncertain significance
CFTR, LOC111674463
Single nucleotide variant
Cystic fibrosis
+1 more
GUncertain significance
CFTR, LOC111674463
Single nucleotide variant
(5 prime UTR variant)
CFTR-related disorders
+4 more
GBenign/Likely benign
LOC111674463, CFTR
Single nucleotide variant
not specified
+3 more
GBenign/Likely benign
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