Variant (rsID / SNP)
rs35767
rs35767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGF1. Location: chromosome 12, position 102,875,569. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- upstream_gene_variant
- Chromosome / position
- 12:102875569
- HGVS
- NM_001111285.3,c.-1410T>C
Associated conditions / phenotypes
Osteoporosis|Bone Mineral Density Quantitative Trait Locus 15|Bone Mineral Density Quantitative Trait Locus 8|Type 2 Diabetes Mellitus|Colorectal Cancer|Diabetes Mellitus|Insulin-Like Growth Factor I|Microvascular Complications of Diabetes 5|Deficiency Anemia|Osteoarthritis|Osteonecrosis|Cardiovascular System Disease|Body Mass Index Quantitative Trait Locus 11|Aging|Multiple Acyl-Coa Dehydrogenase Deficiency|Adult Respiratory Distress Syndrome|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.