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rs2545801

From SNPedia

Orientationminus
Stabilizedminus
Make rs2545801(A;A)
Make rs2545801(A;G)
Make rs2545801(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position177414338
is asnp
is mentioned by
dbSNPrs2545801
ebirs2545801
HLIrs2545801
Exacrs2545801
Varsomers2545801
Maprs2545801
PheGenIrs2545801
hapmaprs2545801
1000 genomesrs2545801
hgdprs2545801
ensemblrs2545801
gopubmedrs2545801
geneviewrs2545801
scholarrs2545801
googlers2545801
pharmgkbrs2545801
gwascentralrs2545801
openSNPrs2545801
23andMers2545801
23andMe allrs2545801
SNP Nexus

SNPshotrs2545801
SNPdbers2545801
MSV3drs2545801
GWAS Ctlgrs2545801
GMAF0.483
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22286219OA-icon.png]
Trait
Title Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
Risk Allele
P-val 9E-11
Odds Ratio 0.1200 None
GWAS snp
PMID [PMID 22703881OA-icon.png]
Trait
Title Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
Risk Allele C
P-val 6E-88
Odds Ratio 1.6800 None


[PMID 27656708] Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels.