Variant (rsID / SNP)
rs1695
rs1695 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSTP1. Location: chromosome 11, position 67,352,689. Clinical significance in the table: Benign.
Reference-table entries
GSTP1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:67352689
- Cytoband
- 11q13.2
- HGVS
- NM_000852.4(GSTP1):c.313A>G (p.Ile105Val)
- Allele change
- Missense_I188V
Associated conditions / phenotypes
Neoplasm of the large intestine|Abnormality of immune system physiology
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.