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rs4790333

From SNPedia

Orientationplus
Stabilizedplus
Make rs4790333(C;C)
Make rs4790333(C;T)
Make rs4790333(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position2359409
GeneSGSM2
is asnp
is mentioned by
dbSNPrs4790333
ebirs4790333
HLIrs4790333
Exacrs4790333
Varsomers4790333
Maprs4790333
PheGenIrs4790333
hapmaprs4790333
1000 genomesrs4790333
hgdprs4790333
ensemblrs4790333
gopubmedrs4790333
geneviewrs4790333
scholarrs4790333
googlers4790333
pharmgkbrs4790333
gwascentralrs4790333
openSNPrs4790333
23andMers4790333
23andMe allrs4790333
SNP Nexus

SNPshotrs4790333
SNPdbers4790333
MSV3drs4790333
GWAS Ctlgrs4790333
GMAF0.4835
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21873549OA-icon.png]
Trait
Title Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
Risk Allele T
P-val 3E-9
Odds Ratio None None