Variant (rsID / SNP)
rs1109866
rs1109866 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB6. Location: chromosome 2, position 220,083,279. The table records no clinical significance for this variant.
Reference-table entries
ABCB6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:220083279
- HGVS
- NM_005689.4,c.117G>A,p.Leu39Leu
- Allele change
- Synonymous_L39L
Associated conditions / phenotypes
Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.