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Links from PubMed

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTN
(R3120Q +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive limb-girdle muscular dystrophy type 2J
+10 more
GConflicting classifications of pathogenicity
ABCC9
Single nucleotide variant
(intron variant)
not specified
+4 more
GConflicting classifications of pathogenicity
PKP2
Single nucleotide variant
(intron variant)
Arrhythmogenic right ventricular dysplasia 9
+3 more
GBenign
LAMA4
(R1073Q +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
LAMA4
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
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