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rs10255329

From SNPedia

Orientationplus
Stabilizedplus
Make rs10255329(C;C)
Make rs10255329(C;G)
Make rs10255329(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position13400597
is asnp
is mentioned by
dbSNPrs10255329
ebirs10255329
HLIrs10255329
Exacrs10255329
Varsomers10255329
Maprs10255329
PheGenIrs10255329
hapmaprs10255329
1000 genomesrs10255329
hgdprs10255329
ensemblrs10255329
gopubmedrs10255329
geneviewrs10255329
scholarrs10255329
googlers10255329
pharmgkbrs10255329
gwascentralrs10255329
openSNPrs10255329
23andMers10255329
23andMe allrs10255329
SNP Nexus

SNPshotrs10255329
SNPdbers10255329
MSV3drs10255329
GWAS Ctlgrs10255329
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23934736OA-icon.png]
Trait Metabolite levels (X-11787)
Title Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study.
Risk Allele C
P-val 7E-6
Odds Ratio .06 [0.03-0.08] unit decrease