Variant (rsID / SNP)

rs761211705

rs761211705 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN3. Location: chromosome 15, position 42,682,142. Clinical significance in the table: Pathogenic.

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Reference-table entries

CAPN3Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 15:42682142
Cytoband: 15q15.1
HGVS: NM_000070.3(CAPN3):c.802-9G>A
Allele change: Silent

Associated conditions / phenotypes

Autosomal recessive limb-girdle muscular dystrophy type 2A

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.