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rs10861032

From SNPedia

Orientationplus
Stabilizedplus
Make rs10861032(C;C)
Make rs10861032(C;T)
Make rs10861032(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position103518728
is asnp
is mentioned by
dbSNPrs10861032
ebirs10861032
HLIrs10861032
Exacrs10861032
Varsomers10861032
Maprs10861032
PheGenIrs10861032
hapmaprs10861032
1000 genomesrs10861032
hgdprs10861032
ensemblrs10861032
gopubmedrs10861032
geneviewrs10861032
scholarrs10861032
googlers10861032
pharmgkbrs10861032
gwascentralrs10861032
openSNPrs10861032
23andMers10861032
23andMe allrs10861032
SNP Nexus

SNPshotrs10861032
SNPdbers10861032
MSV3drs10861032
GWAS Ctlgrs10861032
GMAF0.2847
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21878436OA-icon.png]
Trait
Title A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.
Risk Allele C
P-val 1E-7
Odds Ratio None None