Variant (rsID / SNP)
rs6214
rs6214 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGF1. Location: chromosome 12, position 102,793,569. Clinical significance in the table: Benign.
Reference-table entries
IGF1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:102793569
- Cytoband
- 12q23.2
- HGVS
- NM_000618.5(IGF1):c.*2716G>A
- Allele change
- Silent
Associated conditions / phenotypes
Growth delay due to insulin-like growth factor type 1 deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.