Variant (rsID / SNP)

rs35889956

rs35889956 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN3. Location: chromosome 15, position 42,680,003. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CAPN3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:42680003
Cytoband: 15q15.1
HGVS: NM_000070.3(CAPN3):c.551C>T (p.Thr184Met)
Allele change: Missense_T184M

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.