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Variant (rsID / SNP)

rs754704023

LDB3

rs754704023 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDB3. Location: chromosome 10, position 88,445,421. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LDB3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:88445421
Cytoband
10q23.2
HGVS
NM_007078.3(LDB3):c.689+3861C>T
Allele change
Silent

Associated conditions / phenotypes

Dilated Cardiomyopathy, Dominant|Myofibrillar Myopathy, Dominant|Myofibrillar myopathy 4|Left ventricular noncompaction cardiomyopathy

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.