Variant (rsID / SNP)

rs11199065

rs11199065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BAG3. Location: chromosome 10, position 121,437,329. Clinical significance in the table: Benign.

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Reference-table entries

BAG3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:121437329
Cytoband: 10q26.11
HGVS: NM_004281.4(BAG3):c.*535A>G
Allele change: Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6

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.