Have questions? Visit https://www.reddit.com/r/SNPedia

rs6769511

From SNPedia

Orientationplus
Stabilizedplus
Make rs6769511(C;C)
Make rs6769511(C;T)
Make rs6769511(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position185812502
GeneIGF2BP2
is asnp
is mentioned by
dbSNPrs6769511
ebirs6769511
HLIrs6769511
Exacrs6769511
Varsomers6769511
Maprs6769511
PheGenIrs6769511
hapmaprs6769511
1000 genomesrs6769511
hgdprs6769511
ensemblrs6769511
gopubmedrs6769511
geneviewrs6769511
scholarrs6769511
googlers6769511
pharmgkbrs6769511
gwascentralrs6769511
openSNPrs6769511
23andMers6769511
23andMe allrs6769511
SNP Nexus

SNPshotrs6769511
SNPdbers6769511
MSV3drs6769511
GWAS Ctlgrs6769511
GMAF0.4128
Max Magnitude
? (C;C) (C;T) (T;T) 28
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-9
Odds Ratio 1.23 [1.15-1.31]



GET Evidence
rs6769511
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.453125
summary