Variant (rsID / SNP)
rs9908677
rs9908677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSG1L2. Location: chromosome 17, position 9,712,255. The table records no clinical significance for this variant.
Reference-table entries
GSG1L2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:9712255
- HGVS
- NM_001310219.2,c.403C>T,p.Leu135Leu
- Allele change
- Synonymous_L135L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.