Variant (rsID / SNP)
rs4619
rs4619 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGFBP1. Location: chromosome 7, position 45,932,669. The table records no clinical significance for this variant.
Reference-table entries
IGFBP1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:45932669
- HGVS
- NM_000596.4,c.759A>G,p.Ile253Met
- Allele change
- Missense_I253M
Associated conditions / phenotypes
Adult Respiratory Distress Syndrome|Body Mass Index Quantitative Trait Locus 1|Gastric Cancer|Toxic Shock Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.