Variant (rsID / SNP)
rs9383921
rs9383921 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAET1E. Location: chromosome 6, position 150,210,685. The table records no clinical significance for this variant.
Reference-table entries
RAET1ENot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:150210685
- HGVS
- NM_001394057.1,c.421G>A,p.Ala141Thr
- Allele change
- Silent
Associated conditions / phenotypes
Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.