Variant (rsID / SNP)
rs8187707
rs8187707 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC2. Location: chromosome 10, position 101,610,533. Clinical significance in the table: Benign.
Reference-table entries
ABCC2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:101610533
- Cytoband
- 10q24.2
- HGVS
- NM_000392.5(ABCC2):c.4488C>T (p.His1496=)
- Allele change
- Synonymous_H1496H
Associated conditions / phenotypes
Dubin-Johnson syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.