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rs10953541

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs10953541(C;T)
Make rs10953541(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position107604100
GeneBCAP29
is asnp
is mentioned by
dbSNPrs10953541
ebirs10953541
HLIrs10953541
Exacrs10953541
Varsomers10953541
Maprs10953541
PheGenIrs10953541
hapmaprs10953541
1000 genomesrs10953541
hgdprs10953541
ensemblrs10953541
gopubmedrs10953541
geneviewrs10953541
scholarrs10953541
googlers10953541
pharmgkbrs10953541
gwascentralrs10953541
openSNPrs10953541
23andMers10953541
23andMe allrs10953541
SNP Nexus

SNPshotrs10953541
SNPdbers10953541
MSV3drs10953541
GWAS Ctlgrs10953541
GMAF0.1368
Max Magnitude0
? (C;C) (C;T) (T;T) 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 3E-8
Odds Ratio 1.0800 [1.05-1.11]


[PMID 24825461OA-icon.png] Genetic influences on hand osteoarthritis in Finnish women--a replication study of candidate genes