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rs17586756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17586756(C;T)
Make rs17586756(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position118072882
is asnp
is mentioned by
dbSNPrs17586756
ebirs17586756
HLIrs17586756
Exacrs17586756
Varsomers17586756
Maprs17586756
PheGenIrs17586756
hapmaprs17586756
1000 genomesrs17586756
hgdprs17586756
ensemblrs17586756
gopubmedrs17586756
geneviewrs17586756
scholarrs17586756
googlers17586756
pharmgkbrs17586756
gwascentralrs17586756
openSNPrs17586756
23andMers17586756
23andMe allrs17586756
SNP Nexus

SNPshotrs17586756
SNPdbers17586756
MSV3drs17586756
GWAS Ctlgrs17586756
GMAF0.04086
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19360016OA-icon.png] INSIG2 SNPs Associated With Obesity and Glucose Homeostasis Traits in Hispanics: The IRAS Family Study