Variant (rsID / SNP)
rs387906909
rs387906909 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB6. Location: chromosome 2, position 220,075,813. Clinical significance in the table: Affects.
Reference-table entries
ABCB6Other
- Clinical significance (as recorded)
- Affects
- Variant type
- Microsatellite
- Chromosome / position
- 2:220075813
- Cytoband
- 2q35
- HGVS
- NM_005689.4(ABCB6):c.1985_1986del (p.Leu662fs)
Associated conditions / phenotypes
Langereis blood group
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.