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rs7305618

From SNPedia

Orientationplus
Stabilizedplus
Make rs7305618(C;C)
Make rs7305618(C;T)
Make rs7305618(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120965129
is asnp
is mentioned by
dbSNPrs7305618
ebirs7305618
HLIrs7305618
Exacrs7305618
Varsomers7305618
Maprs7305618
PheGenIrs7305618
hapmaprs7305618
1000 genomesrs7305618
hgdprs7305618
ensemblrs7305618
gopubmedrs7305618
geneviewrs7305618
scholarrs7305618
googlers7305618
pharmgkbrs7305618
gwascentralrs7305618
openSNPrs7305618
23andMers7305618
23andMe allrs7305618
SNP Nexus

SNPshotrs7305618
SNPdbers7305618
MSV3drs7305618
GWAS Ctlgrs7305618
GMAF0.3512
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21647738OA-icon.png]
Trait
Title Genome-wide Association with C-Reactive Protein Levels in CLHNS: Evidence for the CRP and HNF1A Loci and their Interaction with Exposure to a Pathogenic Environment.
Risk Allele T
P-val 1E-8
Odds Ratio 0.2670 [0.18-0.36] unit increase
GWAS snp
PMID [PMID 21573907OA-icon.png]
Trait
Title Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas.
Risk Allele C
P-val 2E-8
Odds Ratio 1.1400 [1.09-1.20]


[PMID 18439552OA-icon.png] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.