Variant (rsID / SNP)

rs12570065

rs12570065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD26. Location: chromosome 10, position 27,293,086. Clinical significance in the table: Benign.

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Reference-table entries

ANKRD26Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:27293086
Cytoband: 10p12.1
HGVS: NM_014915.3(ANKRD26):c.*1433A>G
Allele change: Silent

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.