Variant (rsID / SNP)
rs17883901
rs17883901 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCLC. Location: chromosome 6, position 53,410,037. Clinical significance in the table: Benign.
Reference-table entries
GCLCBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:53410037
- Cytoband
- 6p12.1
- HGVS
- NM_001498.4(GCLC):c.-594C>T
Associated conditions / phenotypes
Myocardial infarction, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.