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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCN7
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
CLCN7
(V418M +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
CLCN7
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
CLCN7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CLCN7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CLCN7
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign
CLCN7
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
CLCN7
Single nucleotide variant
(synonymous variant)
CLCN7-related condition
+2 more
GConflicting classifications of pathogenicity
CLCN7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CLCN7, LOC130058166
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign
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