Variant (rsID / SNP)
rs10741021
rs10741021 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTF1A. Location: chromosome 10, position 23,452,642. Clinical significance in the table: Benign.
Reference-table entries
PTF1ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:23452642
- Cytoband
- 10p12.2
- HGVS
- NC_000010.10:g.23452642A>G
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.