Variant (rsID / SNP)
rs7259041
rs7259041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARRDC2. Location: chromosome 19, position 18,123,738. The table records no clinical significance for this variant.
Reference-table entries
ARRDC2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:18123738
- HGVS
- NM_015683.2,c.1187T>C,p.Leu396Pro
- Allele change
- Missense_L391P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.