Variant (rsID / SNP)
rs3812316
rs3812316 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLXIPL. Location: chromosome 7, position 73,020,337. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 7:73020337
- HGVS
- NM_032951.3,c.723G>C,p.Gln241His
- Allele change
- Missense_Q241H
Associated conditions / phenotypes
Hypertriglyceridemia 1|Hypertriglyceridemia, Transient Infantile|Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Hypercholesterolemia, Familial, 1|Hypercholesterolemia, Familial, 3|Myocardial Infarction|Lipid Metabolism Disorder|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
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.