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rs7607980

From SNPedia

Orientationplus
Stabilizedplus
Make rs7607980(C;C)
Make rs7607980(C;T)
Make rs7607980(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position164694691
GeneCOBLL1
is asnp
is mentioned by
dbSNPrs7607980
dbSNP (classic)rs7607980
ClinGenrs7607980
ebirs7607980
HLIrs7607980
Exacrs7607980
Gnomadrs7607980
Varsomers7607980
LitVarrs7607980
Maprs7607980
PheGenIrs7607980
Biobankrs7607980
1000 genomesrs7607980
hgdprs7607980
ensemblrs7607980
geneviewrs7607980
scholarrs7607980
googlers7607980
pharmgkbrs7607980
gwascentralrs7607980
openSNPrs7607980
23andMers7607980
SNPshotrs7607980
SNPdbers7607980
MSV3drs7607980
GWAS Ctlgrs7607980
GMAF0.1134
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22581228OA-icon.png]
Trait
Title A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
Risk Allele
P-val 4E-20
Odds Ratio None None



[PMID 20031564OA-icon.png] Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.


[PMID 23160641OA-icon.png] Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.


[PMID 23463496OA-icon.png] The COBLL1 C allele is associated with lower serum insulin levels and lower insulin resistance in overweight and obese children.


[PMID 28258026] Replication of newly identified type 2 diabetes susceptible loci in Northwest Indian population.