rs55672373

This is a intron variant variant in the ABCC2 gene.

GWAS Catalog Trait Associations (4)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

X-21467 measurement

Allele T
OR 0.49
p 3.0e-51
N 8,195
Large GWAS
European

glycocholenate sulfate measurement

Feofanova EV et al. Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nature Communications 14(1):3111 (2023)
Allele T
OR 0.41
p 2.0e-36
N 9,016
Large GWAS
multi-ancestry

metabolite measurement

Allele T
OR 0.45
p 5.0e-13
N 2,466
Large GWAS
multi-ancestry

X-24588 measurement

Allele T
OR 0.16
p 2.0e-11
N 4,869
Large GWAS
European

About ABCC2

The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport. Substrates include anticancer drugs such as vinblastine; therefore, this protein appears to contribute to drug resistance in mammalian cells. Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. [provided by RefSeq, Jul 2008]

View all ABCC2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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