Have questions? Visit https://www.reddit.com/r/SNPedia

rs796127

From SNPedia

Orientationminus
Stabilizedminus
Make rs796127(A;A)
Make rs796127(A;G)
Make rs796127(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position31679801
is asnp
is mentioned by
dbSNPrs796127
ebirs796127
HLIrs796127
Exacrs796127
Varsomers796127
Maprs796127
PheGenIrs796127
hapmaprs796127
1000 genomesrs796127
hgdprs796127
ensemblrs796127
gopubmedrs796127
geneviewrs796127
scholarrs796127
googlers796127
pharmgkbrs796127
gwascentralrs796127
openSNPrs796127
23andMers796127
23andMe allrs796127
SNP Nexus

SNPshotrs796127
SNPdbers796127
MSV3drs796127
GWAS Ctlgrs796127
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24763700OA-icon.png]
Trait C-reactive protein levels
Title New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis.
Risk Allele T
P-val 3E-6
Odds Ratio .09 [NR] unit decrease