U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLNC, FLNC-AS1
(A1792V +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
Dilated Cardiomyopathy, Dominant
+6 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
(R1860C +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+8 more
GBenign/Likely benign
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 26
+6 more
GBenign
FLNC, FLNC-AS1
(I1882V +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+8 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 26
+6 more
GBenign
FLNC, FLNC-AS1
(A1922T +1 more)
Single nucleotide variant
(missense variant)
not specified
+7 more
GBenign
FLNC, FLNC-AS1
Single nucleotide variant
(intron variant)
Dilated Cardiomyopathy, Dominant
+5 more
GBenign
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+7 more
GBenign/Likely benign
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
Myofibrillar myopathy 5
+4 more
GConflicting classifications of pathogenicity
FLNC-AS1, FLNC
Single nucleotide variant
(synonymous variant)
Myofibrillar myopathy 5
+6 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
Dilated Cardiomyopathy, Dominant
+6 more
GBenign
FLNC, FLNC-AS1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 26
+4 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
FLNC-related condition
+7 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
(E2270K +1 more)
Single nucleotide variant
(missense variant)
FLNC-related condition
+7 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
(V2331M +1 more)
Single nucleotide variant
(missense variant)
not provided
+6 more
GBenign/Likely benign
FLNC, FLNC-AS1
Single nucleotide variant
(intron variant)
Myofibrillar myopathy 5
+6 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
(R2364H +1 more)
Single nucleotide variant
(missense variant)
FLNC-related condition
+8 more
GBenign/Likely benign
FLNC, FLNC-AS1
(A2430V +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
+6 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
(V2431M +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 26
+5 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
(S2461N +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GUncertain significance
FLNC, FLNC-AS1
(R2621Q +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
(M2668T +1 more)
Single nucleotide variant
(missense variant)
not specified
+7 more
GConflicting classifications of pathogenicity
FLNC, FLNC-AS1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination