Variant (rsID / SNP)
rs375814
rs375814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAB20. Location: chromosome 13, position 111,176,519. The table records no clinical significance for this variant.
Reference-table entries
RAB20Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:111176519
- HGVS
- NM_017817.3,c.198C>A,p.Gly66Gly
- Allele change
- Synonymous_G66G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
