Variant (rsID / SNP)

rs41279942

rs41279942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD26. Location: chromosome 10, position 27,381,397. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ANKRD26Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:27381397
Cytoband: 10p12.1
HGVS: NM_014915.3(ANKRD26):c.576G>A (p.Gln192=)
Allele change: Synonymous_Q192Q

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.