Variant (rsID / SNP)
rs512770
rs512770 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABO. Location: chromosome 9, position 136,133,506. The table records no clinical significance for this variant.
Reference-table entries
ABONot classified
- Variant type
- missense_variant
- Chromosome / position
- 9:136133506
- HGVS
- NM_020469.3,c.220T>C,p.Ser74Pro
- Allele change
- Missense_S74P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.