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rs2237897

From SNPedia

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Geno Mag Summary
(C;C) 0 common
(C;T) 1.2 1.2x increased risk for diabetic nephropathy in some populations
(T;T) 1.4 1.4x increased risk for diabetic nephropathy in some populations
ReferenceGRCh38 38.1/141
Chromosome11
Position2837316
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs2237897
ebirs2237897
HLIrs2237897
Exacrs2237897
Varsomers2237897
Maprs2237897
PheGenIrs2237897
hapmaprs2237897
1000 genomesrs2237897
hgdprs2237897
ensemblrs2237897
gopubmedrs2237897
geneviewrs2237897
scholarrs2237897
googlers2237897
pharmgkbrs2237897
gwascentralrs2237897
openSNPrs2237897
23andMers2237897
23andMe allrs2237897
SNP Nexus

SNPshotrs2237897
SNPdbers2237897
MSV3drs2237897
GWAS Ctlgrs2237897
GMAF0.1589
Max Magnitude1.4
? (C;C) (C;T) (T;T) 28
nature type-2 diabetes
  • rs2237897, P = 6.8 times 10-13; OR = 1.41, 95% CI = 1.29–1.55)

A study of 754 type-2 diabetes patients plus a meta-analysis concluded that rs2237897(T) was significantly associated with susceptibility to diabetic nephropathy in T2D Japanese subjects (odds ratio = 1.22, CI: 1.10-1.34, corrected p = 0.01).[PMID 20056949OA-icon.png]


[PMID 19366866OA-icon.png] Association of type 2 diabetes candidate polymorphisms in KCNQ1 with incretin and insulin secretion

GWAS snp
PMID [PMID 18711366]
Trait Type 2 diabetes
Title SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
Risk Allele C
P-val 1E-16
Odds Ratio 1.33 [1.24-1.41]

[PMID 19448982OA-icon.png] Variants in KCNQ1 are associated with susceptibility to type 2 diabetes in the population of mainland China

[PMID 19516902OA-icon.png] The type 2 diabetes associated minor allele of rs2237895 KCNQ1 associates with reduced insulin release following an oral glucose load


[PMID 19575309] Association study of four variants in KCNQ1 with type 2 diabetes mellitus and premature coronary artery disease in a Chinese population

[PMID 19308350] Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population


[PMID 19252135OA-icon.png] Genetic variation in KCNQ1 associates with fasting glucose and beta-cell function: a study of 3,734 subjects comprising three ethnicities living in Singapore.

[PMID 19556355] Common variants in KCNQ1 are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.

[PMID 20174558OA-icon.png] A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.

[PMID 20701788OA-icon.png] KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population.

[PMID 21261977OA-icon.png] Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US.

[PMID 21289621] Effects of KCNQ1 polymorphisms on the therapeutic efficacy of oral antidiabetic drugs in Chinese patients with type 2 diabetes.

[PMID 21767287] Replication of genome-wide association signals of type 2 diabetes in Han Chinese in a prospective cohort.


[PMID 22696034] KCNQ1 SNPS and susceptibility to diabetic nephropathy in East Asians with type 2 diabetes.


GET Evidence
rs2237897
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0983607
summary



[PMID 23271129] Meta-analysis of the effect of KCNQ1 gene polymorphism on the risk of type 2 diabetes


[PMID 23786590] Common Variants in KCNQ1 Confer Increased Risk of Type 2 Diabetes and Contribute to the Diabetic Epidemic in East Asians: A Replication and Meta-Analysis


[PMID 23298195] Association study of genetic variants of 17 diabetes-related genes/loci and cardiovascular risk and diabetic nephropathy in the Chinese She population.


[PMID 23544998OA-icon.png] Association of TRPC1 gene polymorphisms with type 2 diabetes and diabetic nephropathy in Han Chinese population.

GWAS snp
PMID [PMID 24390345OA-icon.png]
Trait Type 2 diabetes
Title Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
Risk Allele C
P-val 9E-15
Odds Ratio 1.31 [1.22-1.41]


[PMID 25749274] Joint effect of CENTD2 and KCNQ1 polymorphisms on the risk of type 2 diabetes mellitus among chinese han population