Variant (rsID / SNP)
rs7632
rs7632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLF11. Location: chromosome 2, position 10,194,487. Clinical significance in the table: Benign.
Reference-table entries
KLF11Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:10194487
- Cytoband
- 2p25.1
- HGVS
- NM_003597.5(KLF11):c.*1853T>C
- Allele change
- Silent
Associated conditions / phenotypes
Maturity-onset diabetes of the young type 7
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.