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rs687621

From SNPedia

Orientationminus
Stabilizedplus
Make rs687621(C;C)
Make rs687621(C;T)
Make rs687621(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position133261662
GeneABO
is asnp
is mentioned by
dbSNPrs687621
ebirs687621
HLIrs687621
Exacrs687621
Varsomers687621
Maprs687621
PheGenIrs687621
hapmaprs687621
1000 genomesrs687621
hgdprs687621
ensemblrs687621
gopubmedrs687621
geneviewrs687621
scholarrs687621
googlers687621
pharmgkbrs687621
gwascentralrs687621
openSNPrs687621
23andMers687621
23andMe allrs687621
SNP Nexus

SNPshotrs687621
SNPdbers687621
MSV3drs687621
GWAS Ctlgrs687621
GMAF0.3733
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21502573OA-icon.png]
Trait
Title Genetic predictors of fibrin D-dimer levels in healthy adults.
Risk Allele G
P-val 0.000007
Odds Ratio 0.0284 [NR] % increase

[PMID 18604267OA-icon.png] Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.


[PMID 19648918OA-icon.png] Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.

GWAS snp
PMID [PMID 22703881OA-icon.png]
Trait
Title Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
Risk Allele A
P-val 9E-100
Odds Ratio 0.8170 None
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 G
P-val 2E-52
Odds Ratio 1.55 [1.47-1.64]