Variant (rsID / SNP)

rs267607001

rs267607001 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBM20. Location: chromosome 10, position 112,572,056. Clinical significance in the table: Pathogenic.

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Reference-table entries

RBM20Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 10:112572056
Cytoband: 10q25.2
HGVS: NM_001134363.3(RBM20):c.1901G>A (p.Arg634Gln)
Allele change: Missense_R634Q

Associated conditions / phenotypes

Dilated cardiomyopathy 1DD

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.