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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYOM1
(P1600L +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
MYOM1
(I1459K +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GLikely benign
MYOM1
(I1383T +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
MYOM1
(S1236R +1 more)
Single nucleotide variant
(missense variant)
Cardiac arrest
GUncertain significance
MYOM1
(R1231C +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+1 more
GUncertain significance
MYOM1
(H1064Y +1 more)
Single nucleotide variant
(missense variant)
Sudden cardiac death
+2 more
GConflicting classifications of pathogenicity
MYOM1
(R713H)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular cardiomyopathy
+2 more
GUncertain significance
MYOM1
(P660A)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
MYOM1
(R578H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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