Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs34656239

BAG3

rs34656239 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BAG3. Location: chromosome 10, position 121,436,502. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

BAG3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:121436502
Cytoband
10q26.11
HGVS
NM_004281.4(BAG3):c.1436C>T (p.Ala479Val)
Allele change
Missense_A479V

Associated conditions / phenotypes

Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6

Public references

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