Role of ABCG8 D19H (rs11887534) variant in gallstone susceptibility in northern India.

doi:10.1111/j.1440-1746.2010.06349.x

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Role of ABCG8 D19H (rs11887534) variant in gallstone susceptibility in northern India.

Journal of gastroenterology and hepatology - 1 Nov 2010

Srivastava Anshika, Srivastava Anvesha, Srivastava Kshitij, Choudhuri Gourdas, Mittal Balraj

Abstract excerpt

BACKGROUND AND AIM: The excretion of cholesterol from the liver is regulated by the ATP-binding cassette transporter ABCG8. A common genetic polymorphism D19H of ABCG8 might be related to the genetic predisposition of gallstone disease, which is causatively related to supersaturation of cholesterol in bile. We aimed to examine the role of the ABCG8 D19H (rs11887534) polymorphism in susceptibility to gallstone...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to ATP Binding Cassette Transporter, Subfamily G, Member 8

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to ATP-Binding Cassette Transporters

Share to Chi-Square Distribution

Share to Cholesterol

Share to Gallstones

Share to India

Share to Logistic Models

Share to Sex Factors

Source

Open in PubMed

Identifiers

PMID: 21039838
DOI: 10.1111/j.1440-1746.2010.06349.x

Genes

ABCG8

Variants

rs11887534

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Role of ABCG8 D19H (rs11887534) variant in gallstone susceptibility in northern India.PMID 21039838Read ↗

Single nucleotide polymorphism in the ABCG8 transporter gene is associated with gallbladder cancer susceptibility.Semantic proximity Read ↗

Hepatic cholesterol transporter ABCG8 polymorphisms in gallstone disease in an Indian population.Semantic proximity Read ↗

Sterol transporter adenosine triphosphate-binding cassette transporter G8, gallstones, and biliary cancer in 62,000 individuals from the general population.Semantic proximity Read ↗

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.Semantic proximity Read ↗

Gallstone disease in Swedish twins: risk is associated with ABCG8 D19H genotype.Semantic proximity Read ↗

The ABCG8 polymorphism increases the risk of gallbladder cancer in the general population and gallstones in obese patients from Poland.Semantic proximity Read ↗

Association of three common single nucleotide polymorphisms of ATP binding cassette G8 gene with gallstone disease: a meta-analysis.Semantic proximity Read ↗

Role of the ABCG8 19H risk allele in cholesterol absorption and gallstone disease.Semantic proximity Read ↗

Common variant p.D19H of the hepatobiliary sterol transporter ABCG8 increases the risk of gallstones in children.Semantic proximity Read ↗

Risk of gallstones based on ABCG8 rs11887534 single nucleotide polymorphism among Taiwanese men and women.Semantic proximity Read ↗

Genetics of gallstone disease.Semantic proximity Read ↗

Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.