Variant (rsID / SNP)

rs12420456

rs12420456 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN1, SLC22A20P. Location: chromosome 11, position 64,981,837. The table records no clinical significance for this variant.

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Reference-table entries

CAPN1Not classified

Variant type: downstream_gene_variant
Chromosome / position: 11:64981837
HGVS: NM_001198868.2,c.*3080C>T
Allele change: Silent

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.