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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALKBH8
(R581H +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder, autosomal recessive 71
+1 more
GConflicting classifications of pathogenicity
ALKBH8
(R575H +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder, autosomal recessive 71
GUncertain significance
ALKBH8
(R551* +1 more)
Single nucleotide variant
(nonsense +1 more)
Intellectual developmental disorder, autosomal recessive 71
+1 more
GConflicting classifications of pathogenicity
ALKBH8
(W394*)
Single nucleotide variant
(nonsense +1 more)
Intellectual developmental disorder, autosomal recessive 71
GLikely pathogenic
ALKBH8
(R328*)
Single nucleotide variant
(nonsense +1 more)
Intellectual developmental disorder, autosomal recessive 71
GPathogenic/Likely pathogenic
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