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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCNN1B
(S82C)
Single nucleotide variant
(missense variant)
SCNN1B-related condition
+5 more
GConflicting classifications of pathogenicity
SCNN1B
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign
SCNN1B
(G294S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SCNN1B
(I301M)
Single nucleotide variant
(missense variant)
Liddle syndrome 1
+3 more
GUncertain significance
SCNN1B
(G442V)
Single nucleotide variant
(missense variant)
not specified
+4 more
GBenign
SCNN1B
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
SCNN1B
Single nucleotide variant
(synonymous variant)
Liddle syndrome 1
+4 more
GBenign/Likely benign
SCNN1B
Single nucleotide variant
(synonymous variant)
SCNN1B-related condition
+5 more
GBenign/Likely benign
SCNN1B
(S635N)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
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