rs141949189
This variant is located in the HMBS gene.
▶GWAS Catalog Trait Associations (10)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (10)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
apolipoprotein A 1 measurement
cholesteryl esters to total lipids in IDL percentage
free cholesterol to total lipids in large HDL percentage
free cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement
high density lipoprotein cholesterol measurement
cholesteryl ester measurement, high density lipoprotein cholesterol measurement
cholesteryl esters:total lipids ratio, blood VLDL cholesterol amount
free cholesterol measurement, high density lipoprotein cholesterol measurement
lipid measurement, high density lipoprotein cholesterol measurement
phospholipid level, high density lipoprotein cholesterol measurement
About HMBS
This gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
View all HMBS variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
Community Wiki
No community notes yet for this variant. Sign in to start one.
Comments
Sign in to join the discussion.
Loading comments…