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rs1549318

From SNPedia

Orientationplus
Stabilizedplus
Make rs1549318(C;C)
Make rs1549318(C;T)
Make rs1549318(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position70816808
is asnp
is mentioned by
dbSNPrs1549318
ebirs1549318
HLIrs1549318
Exacrs1549318
Varsomers1549318
Maprs1549318
PheGenIrs1549318
hapmaprs1549318
1000 genomesrs1549318
hgdprs1549318
ensemblrs1549318
gopubmedrs1549318
geneviewrs1549318
scholarrs1549318
googlers1549318
pharmgkbrs1549318
gwascentralrs1549318
openSNPrs1549318
23andMers1549318
23andMe allrs1549318
SNP Nexus

SNPshotrs1549318
SNPdbers1549318
MSV3drs1549318
GWAS Ctlgrs1549318
GMAF0.455
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 2E-10
Odds Ratio None None