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rs13161895

From SNPedia

Orientationplus
Stabilizedplus
Make rs13161895(C;C)
Make rs13161895(C;T)
Make rs13161895(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position180044201
GeneRNF130
is asnp
is mentioned by
dbSNPrs13161895
ebirs13161895
HLIrs13161895
Exacrs13161895
Varsomers13161895
Maprs13161895
PheGenIrs13161895
hapmaprs13161895
1000 genomesrs13161895
hgdprs13161895
ensemblrs13161895
gopubmedrs13161895
geneviewrs13161895
scholarrs13161895
googlers13161895
pharmgkbrs13161895
gwascentralrs13161895
openSNPrs13161895
23andMers13161895
23andMe allrs13161895
SNP Nexus

SNPshotrs13161895
SNPdbers13161895
MSV3drs13161895
GWAS Ctlgrs13161895
GMAF0.1515
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21347282OA-icon.png]
Trait
Title Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele T
P-val 6E-7
Odds Ratio 0.1470 [0.09-0.21] SD increase