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Variant (rsID / SNP)

rs2276568

CAPN13

rs2276568 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN13. Location: chromosome 2, position 30,957,326. The table records no clinical significance for this variant.

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Reference-table entries

CAPN13Not classified
Variant type
missense_variant
Chromosome / position
2:30957326
HGVS
NM_144575.3,c.1787T>C,p.Ile596Thr
Allele change
Missense_I596T

Public references

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