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Items: 26

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYPN
Single nucleotide variant
(synonymous variant +2 more)
Dilated cardiomyopathy 1KK
+3 more
GBenign/Likely benign
MYPN
(A245G)
Single nucleotide variant
(missense variant +2 more)
Cardiovascular phenotype
+4 more
GLikely benign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign/Likely benign
MYPN
(R377Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1KK
+4 more
GConflicting classifications of pathogenicity
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Dilated cardiomyopathy 1KK
+3 more
GBenign/Likely benign
MYPN
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1KK
+1 more
GBenign
MYPN
(E467K +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+2 more
GBenign
MYPN
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1KK
+3 more
GBenign/Likely benign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+1 more
GLikely benign
MYPN
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1KK
+1 more
GBenign/Likely benign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
MYPN-related disorder
+4 more
GBenign/Likely benign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
(G804R +1 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1KK
+3 more
GBenign/Likely benign
MYPN
(P816L +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYPN
(R955Q +1 more)
Single nucleotide variant
(missense variant +1 more)
MYPN-related myopathy
+2 more
GUncertain significance
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Dilated cardiomyopathy 1KK
+2 more
GBenign/Likely benign
MYPN
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+3 more
GBenign
MYPN
(R1042C +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
MYPN
(P1112L +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Dilated cardiomyopathy 1KK
+3 more
GBenign/Likely benign
MYPN
(L1161I +1 more)
Single nucleotide variant
(missense variant +1 more)
Primary dilated cardiomyopathy
+7 more
GConflicting classifications of pathogenicity
MYPN
(V1195M +1 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+1 more
GLikely benign
MYPN
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
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