Variant (rsID / SNP)

rs12359281

rs12359281 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD26. Location: chromosome 10, position 27,353,007. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ANKRD26Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:27353007
Cytoband: 10p12.1
HGVS: NM_014915.3(ANKRD26):c.1273A>G (p.Ile425Val)
Allele change: Missense_I425V

Associated conditions / phenotypes

Thrombocytopenia 2

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.