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rs6764623

From SNPedia

Orientationplus
Stabilizedplus
Make rs6764623(A;A)
Make rs6764623(A;C)
Make rs6764623(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position1004354
is asnp
is mentioned by
dbSNPrs6764623
ebirs6764623
HLIrs6764623
Exacrs6764623
Varsomers6764623
Maprs6764623
PheGenIrs6764623
hapmaprs6764623
1000 genomesrs6764623
hgdprs6764623
ensemblrs6764623
gopubmedrs6764623
geneviewrs6764623
scholarrs6764623
googlers6764623
pharmgkbrs6764623
gwascentralrs6764623
openSNPrs6764623
23andMers6764623
23andMe allrs6764623
SNP Nexus

SNPshotrs6764623
SNPdbers6764623
MSV3drs6764623
GWAS Ctlgrs6764623
GMAF0.3329
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23650146OA-icon.png]
Trait Venous thromboembolism
Title A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Risk Allele C
P-val 2E-6
Odds Ratio 1.18 [1.10-1.26]