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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DMD
(N2912D +7 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign/Likely benign
DMD
(E2910V +7 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
DMD
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 3B
+5 more
GBenign
DMD
(R1745H +5 more)
Single nucleotide variant
(missense variant)
Duchenne muscular dystrophy
+4 more
GBenign
DMD
Single nucleotide variant
(synonymous variant)
Duchenne muscular dystrophy
+5 more
GBenign
DMD
Duplication
(intron variant)
Dilated cardiomyopathy 3B
+4 more
GBenign/Likely benign
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