Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs137852764

CSRP3

rs137852764 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSRP3. Location: chromosome 11, position 19,209,758. Clinical significance in the table: Uncertain significance.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CSRP3Uncertain significance
Clinical significance (as recorded)
Uncertain significance
Variant type
single nucleotide variant
Chromosome / position
11:19209758
Cytoband
11p15.1
HGVS
NM_003476.5(CSRP3):c.206A>G (p.Lys69Arg)
Allele change
Missense_K69R

Associated conditions / phenotypes

Dilated cardiomyopathy 1M|Dilated cardiomyopathy 1M|Hypertrophic cardiomyopathy 12|Cardiovascular phenotype|Hypertrophic cardiomyopathy

Public references

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