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rs1319501

From SNPedia

Orientationplus
Stabilizedplus
Make rs1319501(C;C)
Make rs1319501(C;T)
Make rs1319501(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position106285307
GeneNAMPT
is asnp
is mentioned by
dbSNPrs1319501
ebirs1319501
HLIrs1319501
Exacrs1319501
Varsomers1319501
Maprs1319501
PheGenIrs1319501
hapmaprs1319501
1000 genomesrs1319501
hgdprs1319501
ensemblrs1319501
gopubmedrs1319501
geneviewrs1319501
scholarrs1319501
googlers1319501
pharmgkbrs1319501
gwascentralrs1319501
openSNPrs1319501
23andMers1319501
23andMe allrs1319501
SNP Nexus

SNPshotrs1319501
SNPdbers1319501
MSV3drs1319501
GWAS Ctlgrs1319501
GMAF0.1635
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19948877] Visfatin is increased in chronic kidney disease patients with poor appetite and correlates negatively with fasting serum amino acids and triglyceride levels


[PMID 22251423] NAMPT (visfatin) and AKT1 genetic variants associate with myocardial infarction


[PMID 17003359] Common polymorphisms in the promoter of the visfatin gene (PBEF1) influence plasma insulin levels in a French-Canadian population.


[PMID 20346149OA-icon.png] Visfatin, glucose metabolism and vascular disease: a review of evidence.


[PMID 25716650] Effects of NAMPT polymorphisms and haplotypes on circulating visfatin/NAMPT levels in hypertensive disorders of pregnancy