Variant (rsID / SNP)
rs183455182
rs183455182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIOBP. Location: chromosome 22, position 38,130,827. Clinical significance in the table: Benign.
Reference-table entries
TRIOBPBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 22:38130827
- Cytoband
- 22q13.1
- HGVS
- NM_001039141.3(TRIOBP):c.4484A>T (p.Glu1495Val)
- Allele change
- Missense_E1495V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.