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rs4380028

From SNPedia

Orientationminus
Stabilizedminus
Make rs4380028(A;A)
Make rs4380028(A;G)
Make rs4380028(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position78818751
is asnp
is mentioned by
dbSNPrs4380028
dbSNP (classic)rs4380028
ClinGenrs4380028
ebirs4380028
HLIrs4380028
Exacrs4380028
Gnomadrs4380028
Varsomers4380028
LitVarrs4380028
Maprs4380028
PheGenIrs4380028
Biobankrs4380028
1000 genomesrs4380028
hgdprs4380028
ensemblrs4380028
geneviewrs4380028
scholarrs4380028
googlers4380028
pharmgkbrs4380028
gwascentralrs4380028
openSNPrs4380028
23andMers4380028
SNPshotrs4380028
SNPdbers4380028
MSV3drs4380028
GWAS Ctlgrs4380028
GMAF0.3439
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21378988]
Trait
Title A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Risk Allele C
P-val 4E-9
Odds Ratio 1.0700 [1.05-1.10]


[PMID 24573017] Associations between the CDKN2A/B, ADTRP and PDGFD Polymorphisms and the Development of Coronary Atherosclerosis in Japanese Patients


[PMID 33122452OA-icon.png] Association of polymorphisms in ADAMTS-7 gene with the susceptibility to coronary artery disease - a systematic review and meta-analysis.