Variant (rsID / SNP)
rs6925151
rs6925151 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAET1E. Location: chromosome 6, position 150,210,723. The table records no clinical significance for this variant.
Reference-table entries
RAET1ENot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:150210723
- HGVS
- NM_001394057.1,c.383G>A,p.Arg128His
- 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.