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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861896, MYH6
(V1693M)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 14
+7 more
GConflicting classifications of pathogenicity
LOC126861896, MYH6
(R1664H)
Single nucleotide variant
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GBenign/Likely benign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
LOC126861896, MYH6
Single nucleotide variant
(intron variant)
Atrial septal defect 3
+7 more
GBenign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 14
+4 more
GBenign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign/Likely benign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GBenign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
LOC126861896, MYH6
(H1555Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
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