Variant (rsID / SNP)
rs4740
rs4740 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EBI3. Location: chromosome 19, position 4,236,996. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 19:4236996
- HGVS
- NM_005755.3,c.601G>A,p.Val201Ile
- Allele change
- Missense_V201I
Associated conditions / phenotypes
Heart Disease|Coronary Heart Disease 1|Body Mass Index Quantitative Trait Locus 11|Hypertriglyceridemia 1|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|Hypertriglyceridemia, Transient Infantile|Body Mass Index Quantitative Trait Locus 14|Body Mass Index Quantitative Trait Locus 9|Body Mass Index Quantitative Trait Locus 8|Hypoalphalipoproteinemia|Autoimmune Disease|Mycobacterium Tuberculosis 1|Lipoprotein Quantitative Trait Locus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.