Variant (rsID / SNP)
rs864687
rs864687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RINT1. Location: chromosome 7, position 105,205,917. Clinical significance in the table: Benign.
Reference-table entries
RINT1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:105205917
- Cytoband
- 7q22.3
- HGVS
- NM_021930.6(RINT1):c.2067+13A>C
- Allele change
- Silent
Associated conditions / phenotypes
Infantile liver failure syndrome 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.