Variant (rsID / SNP)

rs371227553

rs371227553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DYSF. Location: chromosome 2, position 71,886,005. Clinical significance in the table: Likely benign.

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Reference-table entries

DYSFLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:71886005
Cytoband: 2p13.2
HGVS: NM_001130987.2(DYSF):c.4756-3C>T
Allele change: Silent

Associated conditions / phenotypes

Qualitative or quantitative defects of dysferlin|Autosomal recessive limb-girdle muscular dystrophy type 2B

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.