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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMN, LOC130056554
Single nucleotide variant
(synonymous variant)
Imerslund-Grasbeck syndrome type 2
+1 more
GLikely benign
AMN, LOC130056554
(A330E)
Single nucleotide variant
(missense variant)
Imerslund-Grasbeck syndrome type 2
+1 more
GConflicting classifications of pathogenicity
AMN, LOC130056554
(G336S)
Single nucleotide variant
(missense variant)
Imerslund-Grasbeck syndrome type 2
+1 more
GUncertain significance
AMN, LOC130056554
(H352Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
AMN, LOC130056554
Deletion
(inframe_deletion)
Imerslund-Grasbeck syndrome type 2
GUncertain significance
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