rs687621

Orientation

minus

Stabilized

minus

Make rs687621(C;C)

Make rs687621(C;T)

Make rs687621(T;T)

Reference

GRCh38 38.1/142

Chromosome

9

Position

133261662

Gene

ABO

is a	snp
is	mentioned by
dbSNP	rs687621
dbSNP (classic)	rs687621
ClinGen	rs687621
ebi	rs687621
HLI	rs687621
Exac	rs687621
Gnomad	rs687621
Varsome	rs687621
LitVar	rs687621
Map	rs687621
PheGenI	rs687621
Biobank	rs687621
1000 genomes	rs687621
hgdp	rs687621
ensembl	rs687621
geneview	rs687621
scholar	rs687621
google	rs687621
pharmgkb	rs687621
gwascentral	rs687621
openSNP	rs687621
23andMe	rs687621
SNPshot	rs687621
SNPdbe	rs687621
MSV3d	rs687621
GWAS Ctlg	rs687621

GMAF

0.3733

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 21502573]
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 18604267] Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.

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

GWAS snp
PMID	[PMID 22703881]
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 23650146]
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]