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Items: 1 to 100 of 169

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RYR2
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(intron variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+2 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(intron variant)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
not provided
+6 more
GConflicting classifications of pathogenicity
RYR2
(I217V)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+5 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
RYR2
(L237P)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Arrhythmogenic right ventricular dysplasia 2
+7 more
GConflicting classifications of pathogenicity
RYR2
(R298C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
RYR2
(G348D)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Arrhythmogenic right ventricular dysplasia 2
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Arrhythmogenic right ventricular dysplasia 2
+6 more
GBenign/Likely benign
RYR2
(R420W)
Single nucleotide variant
(missense variant)
not provided
+6 more
GConflicting classifications of pathogenicity
RYR2
(V452I)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia
+2 more
GUncertain significance
RYR2
(H464Q)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia
+7 more
GConflicting classifications of pathogenicity
RYR2
(R485Q)
Single nucleotide variant
(missense variant)
not specified
+6 more
GUncertain significance
RYR2
Single nucleotide variant
(intron variant)
not provided
+4 more
GConflicting classifications of pathogenicity
RYR2
Duplication
not specified
+2 more
GBenign/Likely benign
RYR2
(R564K)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+6 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(intron variant)
not provided
+6 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+4 more
GBenign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+4 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+7 more
GBenign/Likely benign
RYR2
(R1013W)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
RYR2
(R1013Q)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+6 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GConflicting classifications of pathogenicity
RYR2
(D1070H)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+1 more
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia
+3 more
GLikely benign
RYR2
(R1119H)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
RYR2
(E1127G)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+7 more
GConflicting classifications of pathogenicity
RYR2
(A1136V)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia
+6 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(intron variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+2 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign/Likely benign
RYR2
(V1241I)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
LOC126806067, RYR2
(S1295G)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia
+5 more
GConflicting classifications of pathogenicity
LOC126806067, RYR2
Single nucleotide variant
(synonymous variant)
not provided
+6 more
GConflicting classifications of pathogenicity
LOC126806067, RYR2
(G1324A)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+4 more
GUncertain significance
LOC126806067, RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(intron variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+1 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia
+3 more
GLikely benign
RYR2
(C1489R)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 2
+5 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+6 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+6 more
GBenign/Likely benign
RYR2
(P1583S)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+5 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+3 more
GConflicting classifications of pathogenicity
RYR2
(S1638T)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 1
+4 more
GUncertain significance
RYR2
(E1646D)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Arrhythmogenic right ventricular cardiomyopathy
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
RYR2
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+3 more
GBenign/Likely benign
RYR2
(S1765C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+6 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+5 more
GBenign
RYR2
(R1919W)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia
+4 more
GUncertain significance
RYR2
Single nucleotide variant
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
RYR2
(M1975V)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
RYR2
(G2094S)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+5 more
GUncertain significance
RYR2
(V2113M)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
RYR2
(T2116A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
RYR2
(R2144C)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(intron variant)
not specified
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
RYR2
(S2246L)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+3 more
GPathogenic
RYR2
Single nucleotide variant
(intron variant)
not provided
+5 more
GBenign
RYR2
(A2334T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
RYR2
(I2351T)
Single nucleotide variant
(missense variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+1 more
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+7 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
RYR2
Deletion
(inframe_deletion)
Cardiomyopathy
GLikely pathogenic
RYR2
Single nucleotide variant
(synonymous variant)
Catecholaminergic polymorphic ventricular tachycardia 1
+5 more
GBenign/Likely benign
RYR2
(A2498V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
RYR2
(T2510A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
RYR2
(H2540R)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
RYR2
(E2715D)
Single nucleotide variant
(missense variant)
not specified
+6 more
GConflicting classifications of pathogenicity
RYR2
(I2721T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
RYR2
Single nucleotide variant
(intron variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
RYR2
(R2803Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GConflicting classifications of pathogenicity
RYR2
Duplication
Arrhythmogenic right ventricular cardiomyopathy
+5 more
GBenign/Likely benign
RYR2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+6 more
GBenign
RYR2
(I2898V)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
RYR2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
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