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Variant (rsID / SNP)

rs17596

CAPN2

rs17596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN2. Location: chromosome 1, position 223,905,532. The table records no clinical significance for this variant.

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Reference-table entries

CAPN2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
1:223905532
HGVS
NM_001748.5,c.306G>A,p.Leu102Leu
Allele change
Synonymous_L24L

Public references

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