Variant (rsID / SNP)
rs4938013
rs4938013 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKK1. Location: chromosome 11, position 113,264,470. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 11:113264470
- HGVS
- NM_178510.2,c.453A>C,p.Ile151Ile
- Allele change
- Synonymous_I151I
Associated conditions / phenotypes
Body Mass Index Quantitative Trait Locus 11|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Body Mass Index Quantitative Trait Locus 10|Body Mass Index Quantitative Trait Locus 7|Body Mass Index Quantitative Trait Locus 4|Body Mass Index Quantitative Trait Locus 12|Body Mass Index Quantitative Trait Locus 14|Body Mass Index Quantitative Trait Locus 9|Body Mass Index Quantitative Trait Locus 8|Eating Disorder|Heroin Dependence|Substance Dependence|Opioid Addiction|Drug Dependence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.