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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALS2
Single nucleotide variant
(intron variant)
not provided
+5 more
GBenign
ALS2
(I1373M)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 2, juvenile
+5 more
GBenign/Likely benign
ALS2
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign
ALS2
Single nucleotide variant
(synonymous variant)
Infantile-onset ascending hereditary spastic paralysis
+5 more
GBenign
ALS2
Single nucleotide variant
(synonymous variant)
Infantile-onset ascending hereditary spastic paralysis
+5 more
GBenign
ALS2
Single nucleotide variant
(intron variant)
Amyotrophic lateral sclerosis type 2, juvenile
+5 more
GConflicting classifications of pathogenicity
ALS2
Single nucleotide variant
(synonymous variant)
Hereditary spastic paraplegia
+4 more
GConflicting classifications of pathogenicity
ALS2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
ALS2
(V368M)
Single nucleotide variant
(missense variant)
not provided
+5 more
GBenign
ALS2
(I94V)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia
+5 more
GBenign
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