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Variant (rsID / SNP)

rs508405

CAPN13

rs508405 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN13. Location: chromosome 2, position 30,980,940. The table records no clinical significance for this variant.

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Reference-table entries

CAPN13Not classified
Variant type
missense_variant
Chromosome / position
2:30980940
HGVS
NM_144575.3,c.838G>A,p.Ala280Thr
Allele change
Missense_A280T

Public references

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