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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC24A5
(T111A)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
MYEF2, SLC24A5
Single nucleotide variant
(synonymous variant +1 more)
SLC24A5-related disorder
+1 more
GConflicting classifications of pathogenicity
MYEF2, SLC24A5
(S311Y)
Single nucleotide variant
(missense variant +1 more)
SLC24A5-related disorder
+1 more
GLikely benign
SLC24A5, MYEF2
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+1 more
GBenign
MYEF2, SLC24A5
Single nucleotide variant
(synonymous variant +1 more)
SLC24A5-related disorder
+1 more
GLikely benign
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