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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH11, NDE1
(E1833D +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+5 more
GConflicting classifications of pathogenicity
NDE1, MYH11
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
NDE1, MYH11
Single nucleotide variant
(intron variant)
Stroke disorder
+2 more
GConflicting classifications of pathogenicity
MYH11
(L1243P +1 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GConflicting classifications of pathogenicity
MYH11
(R1114W +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
MYH11
(G695S +1 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GUncertain significance
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