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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC34A3
(S192L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
SLC34A3
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
SLC34A3
(G264S)
Single nucleotide variant
(missense variant)
SLC34A3-related disorder
+3 more
GConflicting classifications of pathogenicity
SLC34A3
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
SLC34A3
(E513V)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
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