Variant (rsID / SNP)
rs34896
rs34896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHOBTB3. Location: chromosome 5, position 95,084,131. The table records no clinical significance for this variant.
Reference-table entries
RHOBTB3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 5:95084131
- HGVS
- NM_014899.4,c.510G>A,p.Ala170Ala
- Allele change
- Synonymous_A170A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.