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rs17047718

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17047718(A;G)
Make rs17047718(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position118079736
is asnp
is mentioned by
dbSNPrs17047718
ebirs17047718
HLIrs17047718
Exacrs17047718
Varsomers17047718
Maprs17047718
PheGenIrs17047718
hapmaprs17047718
1000 genomesrs17047718
hgdprs17047718
ensemblrs17047718
gopubmedrs17047718
geneviewrs17047718
scholarrs17047718
googlers17047718
pharmgkbrs17047718
gwascentralrs17047718
openSNPrs17047718
23andMers17047718
23andMe allrs17047718
SNP Nexus

SNPshotrs17047718
SNPdbers17047718
MSV3drs17047718
GWAS Ctlgrs17047718
GMAF0.08815
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 19360016OA-icon.png] INSIG2 SNPs Associated With Obesity and Glucose Homeostasis Traits in Hispanics: The IRAS Family Study