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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCNN1G
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SCNN1G
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign/Likely benign
SCNN1G
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GConflicting classifications of pathogenicity
SCNN1G
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
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