Variant (rsID / SNP)
rs8100856
rs8100856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP8B3. Location: chromosome 19, position 1,796,166. The table records no clinical significance for this variant.
Reference-table entries
ATP8B3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:1796166
- HGVS
- NM_138813.4,c.1852G>A,p.Val618Ile
- Allele change
- Missense_V618I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.