Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs41303181

DMD

rs41303181 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DMD. Clinical significance in the table: Benign.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

DMDBenign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Cytoband
Xp21.1
HGVS
NM_004006.3(DMD):c.4234-13A>G
Allele change
Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 3B|Duchenne muscular dystrophy|Becker muscular dystrophy|Duchenne muscular dystrophy|Cardiomyopathy|Dystrophin deficiency

Public references

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