Variant (rsID / SNP)
rs6115906
rs6115906 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBCK1. Location: chromosome 20, position 397,928. The table records no clinical significance for this variant.
Reference-table entries
RBCK1Not classified
- Variant type
- intron_variant
- Chromosome / position
- 20:397928
- HGVS
- NM_031229.4,c.168-242C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.