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Variant (rsID / SNP)

rs61735268

RBM20

rs61735268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBM20. Location: chromosome 10, position 112,541,062. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RBM20Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
10:112541062
Cytoband
10q25.2
HGVS
NM_001134363.3(RBM20):c.695G>A (p.Gly232Asp)
Allele change
Missense_G232D

Associated conditions / phenotypes

Cardiovascular phenotype|Dilated cardiomyopathy 1DD|Cardiomyopathy

Public references

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