Variant (rsID / SNP)
rs3818136
rs3818136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D22B. Location: chromosome 6, position 37,252,210. The table records no clinical significance for this variant.
Reference-table entries
TBC1D22BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:37252210
- HGVS
- NM_017772.4,c.771C>T,p.Asn257Asn
- Allele change
- Synonymous_N257N
Associated conditions / phenotypes
Prostate Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.