Variant (rsID / SNP)
rs561612231
rs561612231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB4. Location: chromosome 7, position 87,035,805. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
ABCB4Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:87035805
- Cytoband
- 7q21.12
- HGVS
- NM_000443.4(ABCB4):c.3285C>T (p.Leu1095=)
- Allele change
- Synonymous_L1102L
Associated conditions / phenotypes
Cholestasis, intrahepatic, of pregnancy, 3|Progressive familial intrahepatic cholestasis type 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.