Variant (rsID / SNP)
rs6668857
rs6668857 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHBG. Location: chromosome 1, position 156,354,367. The table records no clinical significance for this variant.
Reference-table entries
RHBGNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:156354367
- HGVS
- NM_020407.5,c.1283A>G,p.His428Arg
- Allele change
- Silent
Associated conditions / phenotypes
Missense_H428R|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.