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rs555212

From SNPedia

Orientationplus
Stabilizedplus
Make rs555212(A;A)
Make rs555212(A;G)
Make rs555212(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113102226
is asnp
is mentioned by
dbSNPrs555212
dbSNP (classic)rs555212
ClinGenrs555212
ebirs555212
HLIrs555212
Exacrs555212
Gnomadrs555212
Varsomers555212
LitVarrs555212
Maprs555212
PheGenIrs555212
Biobankrs555212
1000 genomesrs555212
hgdprs555212
ensemblrs555212
geneviewrs555212
scholarrs555212
googlers555212
pharmgkbrs555212
gwascentralrs555212
openSNPrs555212
23andMers555212
SNPshotrs555212
SNPdbers555212
MSV3drs555212
GWAS Ctlgrs555212
GMAF0.2617
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23381943OA-icon.png]
Trait End-stage coagulation
Title Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
Risk Allele G
P-val 1E-15
Odds Ratio .37 [0.28-0.46] unit decrease


[PMID 20735728OA-icon.png] Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men.