Have questions? Visit https://www.reddit.com/r/SNPedia

rs4591494

From SNPedia

Orientationplus
Stabilizedplus
Make rs4591494(C;C)
Make rs4591494(C;T)
Make rs4591494(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position7941140
is asnp
is mentioned by
dbSNPrs4591494
ebirs4591494
HLIrs4591494
Exacrs4591494
Varsomers4591494
Maprs4591494
PheGenIrs4591494
hapmaprs4591494
1000 genomesrs4591494
hgdprs4591494
ensemblrs4591494
gopubmedrs4591494
geneviewrs4591494
scholarrs4591494
googlers4591494
pharmgkbrs4591494
gwascentralrs4591494
openSNPrs4591494
23andMers4591494
23andMe allrs4591494
SNP Nexus

SNPshotrs4591494
SNPdbers4591494
MSV3drs4591494
GWAS Ctlgrs4591494
GMAF0.275
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs4591494
PubMedID [PMID 17903294OA-icon.png]
Condition Factor VII
Gene Intergenic
Risk Allele
pValue 9.00E-006
OR NA
95% CI



GET Evidence
rs4591494
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary