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rs2774279

From SNPedia

Orientationplus
Stabilizedplus
Make rs2774279(C;C)
Make rs2774279(C;T)
Make rs2774279(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161047766
GeneARHGAP30, USF1
is asnp
is mentioned by
dbSNPrs2774279
ebirs2774279
HLIrs2774279
Exacrs2774279
Varsomers2774279
Maprs2774279
PheGenIrs2774279
hapmaprs2774279
1000 genomesrs2774279
hgdprs2774279
ensemblrs2774279
gopubmedrs2774279
geneviewrs2774279
scholarrs2774279
googlers2774279
pharmgkbrs2774279
gwascentralrs2774279
openSNPrs2774279
23andMers2774279
23andMe allrs2774279
SNP Nexus

SNPshotrs2774279
SNPdbers2774279
MSV3drs2774279
GWAS Ctlgrs2774279
GMAF0.2121
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 18097648] The minor allele of rs2774279 was less common among individuals with metabolic syndrome than among healthy controls [p = 0.0029; p = 0.0073]. The minor allele of rs2774279 was also associated with lower BMI, lower fasting glucose values and higher HDL-cholesterol concentrations in longitudinal analyses.


[PMID 16699592OA-icon.png] Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.


[PMID 18276913OA-icon.png] Association analysis of allelic variants of USF1 in coronary atherosclerosis.


[PMID 18974842OA-icon.png] Gender differences in genetic risk profiles for cardiovascular disease.