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rs10895547

From SNPedia

Orientationplus
Stabilizedplus
Make rs10895547(C;C)
Make rs10895547(C;T)
Make rs10895547(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position103937424
GenePDGFD
is asnp
is mentioned by
dbSNPrs10895547
ebirs10895547
HLIrs10895547
Exacrs10895547
Varsomers10895547
Maprs10895547
PheGenIrs10895547
hapmaprs10895547
1000 genomesrs10895547
hgdprs10895547
ensemblrs10895547
gopubmedrs10895547
geneviewrs10895547
scholarrs10895547
googlers10895547
pharmgkbrs10895547
gwascentralrs10895547
openSNPrs10895547
23andMers10895547
23andMe allrs10895547
SNP Nexus

SNPshotrs10895547
SNPdbers10895547
MSV3drs10895547
GWAS Ctlgrs10895547
GMAF0.3347
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 0.000003
Odds Ratio 0.0747 [0.04-0.10] SD decrease