Variant (rsID / SNP)

rs121908333

rs121908333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDB3. Location: chromosome 10, position 88,446,920. 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: 10:88446920
Cytoband: 10q23.2
HGVS: NM_001368067.1(LDB3):c.439G>A (p.Ala147Thr)
Allele change: Missense_A262T

Associated conditions / phenotypes

Myofibrillar myopathy 4|Cardiomyopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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