Variant (rsID / SNP)
rs35039208
rs35039208 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBGT1. Location: chromosome 9, position 136,030,573. The table records no clinical significance for this variant.
Reference-table entries
GBGT1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:136030573
- HGVS
- NM_021996.6,c.351C>T,p.Ala117Ala
- Allele change
- Synonymous_A100A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.