Variant (rsID / SNP)
rs9908146
rs9908146 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNK. Location: chromosome 17, position 73,812,909. The table records no clinical significance for this variant.
Reference-table entries
UNKNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:73812909
- HGVS
- NM_001080419.3,c.1020A>G,p.Pro340Pro
- Allele change
- Synonymous_P340P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.