Variant (rsID / SNP)
rs2227692
rs2227692 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINE1. Location: chromosome 7, position 100,779,244. The table records no clinical significance for this variant.
Reference-table entries
SERPINE1Not classified
- Variant type
- intron_variant
- Chromosome / position
- 7:100779244
- HGVS
- NM_001386460.1,c.1087+162C>T
- Allele change
- Silent
Associated conditions / phenotypes
Gastric Cancer|Type 2 Diabetes Mellitus|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3|Microvascular Complications of Diabetes 7
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.