Variant (rsID / SNP)
rs1053878
rs1053878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABO. Location: chromosome 9, position 136,131,651. Clinical significance in the table: no interpretation for the single variant.
Reference-table entries
ABOOther
- Clinical significance (as recorded)
- no interpretation for the single variant
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:136131651
- Cytoband
- 9q34.2
- HGVS
- NM_020469.2(ABO):c.467C>T (p.Pro156Leu)
- Allele change
- Missense_R156W
Associated conditions / phenotypes
Thrombosis|Ovarian Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.