Variant (rsID / SNP)
rs1496555
rs1496555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SKI. Location: chromosome 1, position 2,234,251. Clinical significance in the table: Benign.
Reference-table entries
SKIBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:2234251
- Cytoband
- 1p36.32
- HGVS
- NM_003036.4(SKI):c.970-166A>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.