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rs2074196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2074196(G;T)
Make rs2074196(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2803570
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs2074196
ebirs2074196
HLIrs2074196
Exacrs2074196
Varsomers2074196
Maprs2074196
PheGenIrs2074196
hapmaprs2074196
1000 genomesrs2074196
hgdprs2074196
ensemblrs2074196
gopubmedrs2074196
geneviewrs2074196
scholarrs2074196
googlers2074196
pharmgkbrs2074196
gwascentralrs2074196
openSNPrs2074196
23andMers2074196
23andMe allrs2074196
SNP Nexus

SNPshotrs2074196
SNPdbers2074196
MSV3drs2074196
GWAS Ctlgrs2074196
GMAF0.1827
Max Magnitude0
? (G;G) (G;T) (T;T) 28

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


[PMID 19850681] Association of KCNQ1 Polymorphisms with the Gestational Diabetes Mellitus in Korean Women [PMID 19448982OA-icon.png] Variants in KCNQ1 are associated with susceptibility to type 2 diabetes in the population of mainland China.


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


[PMID 20606385] Polymorphisms in KCNQ1 are associated with gestational diabetes in a Korean population.

[PMID 26109524] Role of high-risk variants in the development of impaired glucose metabolism was modified by birth weight in Han Chinese