Variant (rsID / SNP)
rs1061627
rs1061627 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RECQL. Location: chromosome 12, position 21,654,407. Clinical significance in the table: Benign.
Reference-table entries
RECQLBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:21654407
- Cytoband
- 12p12.1
- HGVS
- NM_002907.4(RECQL):c.-349C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.