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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH9
(E1777K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MYH9
(G736R)
Single nucleotide variant
(missense variant)
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
GUncertain significance
MYH9
(R693C)
Single nucleotide variant
(missense variant)
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
+2 more
GUncertain significance
MYH9
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance
MYH9
(W33R)
Single nucleotide variant
(missense variant)
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
GPathogenic
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