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rs561241

From SNPedia

Orientationminus
Stabilizedminus
Make rs561241(A;A)
Make rs561241(A;G)
Make rs561241(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113105720
GeneF7
is asnp
is mentioned by
dbSNPrs561241
ebirs561241
HLIrs561241
Exacrs561241
Varsomers561241
Maprs561241
PheGenIrs561241
hapmaprs561241
1000 genomesrs561241
hgdprs561241
ensemblrs561241
gopubmedrs561241
geneviewrs561241
scholarrs561241
googlers561241
pharmgkbrs561241
gwascentralrs561241
openSNPrs561241
23andMers561241
23andMe allrs561241
SNP Nexus

SNPshotrs561241
SNPdbers561241
MSV3drs561241
GWAS Ctlgrs561241
GMAF0.1028
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 17903294OA-icon.png] risk of cardiovascular disease

rs561241 for hemostatic factors was p = 4.5*10(-16)

[PMID 17903291OA-icon.png] The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.

[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

[PMID 19822575OA-icon.png] Molecular interactions between HNF4a, FOXA2 and GABP identified at regulatory DNA elements through ChIP-sequencing.

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 C
P-val 4E-56
Odds Ratio 0.0350 None


GET Evidence
rs561241
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.119048
summary