Variant (rsID / SNP)
rs73245775
rs73245775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBPJ. Location: chromosome 4, position 26,361,568. Clinical significance in the table: Benign.
Reference-table entries
RBPJBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:26361568
- Cytoband
- 4p15.2
- HGVS
- NM_015874.6(RBPJ):c.21-26407G>A
- Allele change
- Silent
Associated conditions / phenotypes
Type 2 diabetes mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.