Variant (rsID / SNP)

rs104894791

rs104894791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DMD. Clinical significance in the table: Uncertain significance.

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Reference-table entries

DMDUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: Xp21.2
HGVS: NM_004006.3(DMD):c.10262C>T (p.Ala3421Val)
Allele change: Missense_A353V

Associated conditions / phenotypes

Becker muscular dystrophy|Duchenne 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.