Variant (rsID / SNP)
rs8176720
rs8176720 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABO. Location: chromosome 9, position 136,132,873. The table records no clinical significance for this variant.
Reference-table entries
ABONot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:136132873
- HGVS
- NM_020469.3,c.294A>G,p.Thr98Thr
- Allele change
- Missense_H99R
Associated conditions / phenotypes
Thyroid Hyalinizing Trabecular Adenoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.