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Variant (rsID / SNP)

rs139049098

ANKRD26

rs139049098 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD26. Location: chromosome 10, position 27,389,103. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ANKRD26Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:27389103
Cytoband
10p12.1
HGVS
NM_014915.3(ANKRD26):c.153C>G (p.His51Gln)
Allele change
Missense_H51Q

Associated conditions / phenotypes

Thrombocytopenia 2

Public references

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