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Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.

BMC medical genetics - 28 May 2010

Han Xueyao, Luo Yingying, Ren Qian, Zhang Xiuying, Wang Fang, Sun Xiuqin, Zhou Xianghai, Ji Linong

Abstract excerpt

BACKGROUND: Recently, several genome-wide and candidate gene association studies have identified many novel genetic loci for type 2 diabetes (T2D); among these genes, CDKAL1, IGF2BP2, SLC30A8, CDKN2A/B, HHEX, FTO, TCF2, KCNQ1, and WFS1 are the most important. We aimed to determine the effects of these genetic loci associated with T2D in the Chinese Han population of China. METHODS: Single-nucleotide polymorphisms...

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Source

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Identifiers

PMID: 20509872
DOI: 10.1186/1471-2350-11-81
PMCID: PMC2896346

Genes

CDKAL1
FTO
WFS1
HHEX
KCNQ1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.PMID 20509872Read ↗

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