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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A6
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign/Likely benign
SLC12A6
(S471T +4 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
SLC12A6
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
SLC12A6
Deletion
(intron variant)
not provided
GBenign
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