Variant (rsID / SNP)
rs6697248
rs6697248 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STIL. Location: chromosome 1, position 47,766,943. Clinical significance in the table: Benign.
Reference-table entries
STILBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:47766943
- Cytoband
- 1p33
- HGVS
- NM_001048166.1(STIL):c.453+290A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.