Variant (rsID / SNP)
rs2296651
rs2296651 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC10A1. Location: chromosome 14, position 70,245,193. Clinical significance in the table: Benign.
Reference-table entries
SLC10A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:70245193
- Cytoband
- 14q24.1
- HGVS
- NM_003049.4(SLC10A1):c.800C>T (p.Ser267Phe)
- Allele change
- Missense_S267F
Associated conditions / phenotypes
Hypercholanemia, familial, 2|Hepatitis B virus, resistance to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.