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Variant (rsID / SNP)

rs374665929

CAPN3

rs374665929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN3. Location: chromosome 15, position 42,691,681. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

CAPN3Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
15:42691681
Cytoband
15q15.1
HGVS
NM_000070.3(CAPN3):c.1194-9A>G
Allele change
Silent

Associated conditions / phenotypes

Autosomal recessive limb-girdle muscular dystrophy type 2A

Public references

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