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rs2359536

From SNPedia

Orientationplus
Stabilizedplus
Make rs2359536(C;C)
Make rs2359536(C;T)
Make rs2359536(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position20610679
is asnp
is mentioned by
dbSNPrs2359536
ebirs2359536
HLIrs2359536
Exacrs2359536
Varsomers2359536
Maprs2359536
PheGenIrs2359536
hapmaprs2359536
1000 genomesrs2359536
hgdprs2359536
ensemblrs2359536
gopubmedrs2359536
geneviewrs2359536
scholarrs2359536
googlers2359536
pharmgkbrs2359536
gwascentralrs2359536
openSNPrs2359536
23andMers2359536
23andMe allrs2359536
SNP Nexus

SNPshotrs2359536
SNPdbers2359536
MSV3drs2359536
GWAS Ctlgrs2359536
GMAF0.2433
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20610895]
Trait Peripheral artery disease
Title Identification of Evidence Suggestive of an Association with Peripheral Arterial Disease at the OSBPL10 Locus by Genome-Wide Investigation in the Japanese Population
Risk Allele C
P-val 0.000002
Odds Ratio 1.84 [1.43-2.37]