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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM2
Single nucleotide variant
(intron variant)
Autosomal dominant centronuclear myopathy
+3 more
GBenign/Likely benign
DNM2
Single nucleotide variant
(intron variant)
not provided
+4 more
GConflicting classifications of pathogenicity
DNM2
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GBenign/Likely benign
DNM2
(R465W)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic
DNM2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+4 more
GBenign/Likely benign
DNM2
Single nucleotide variant
(intron variant)
not provided
+5 more
GBenign/Likely benign
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