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Variant (rsID / SNP)

rs191746041

DYSF

rs191746041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DYSF. Location: chromosome 2, position 71,825,884. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DYSFConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:71825884
Cytoband
2p13.2
HGVS
NM_001130987.2(DYSF):c.3756+9G>T
Allele change
Silent

Associated conditions / phenotypes

Qualitative or quantitative defects of dysferlin

Public references

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