Variant (rsID / SNP)

rs12444596

rs12444596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CA5A. Location: chromosome 16, position 87,957,748. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CA5ANot classified

Variant type: intron_variant
Chromosome / position: 16:87957748
HGVS: NM_001739.2,c.340+2606G>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.