Variant (rsID / SNP)

rs5972633

rs5972633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DMD. Clinical significance in the table: Benign.

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Reference-table entries

DMDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp21.1
HGVS: NM_004006.3(DMD):c.961-5853C>T
Allele change: Silent

Associated conditions / phenotypes

Cardiomyopathy|Duchenne muscular dystrophy|Dystrophin deficiency|Becker muscular dystrophy

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.