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rs7159841

From SNPedia

Orientationplus
Stabilizedplus
Make rs7159841(C;C)
Make rs7159841(C;T)
Make rs7159841(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position47394632
GeneMDGA2
is asnp
is mentioned by
dbSNPrs7159841
ebirs7159841
HLIrs7159841
Exacrs7159841
Varsomers7159841
Maprs7159841
PheGenIrs7159841
hapmaprs7159841
1000 genomesrs7159841
hgdprs7159841
ensemblrs7159841
gopubmedrs7159841
geneviewrs7159841
scholarrs7159841
googlers7159841
pharmgkbrs7159841
gwascentralrs7159841
openSNPrs7159841
23andMers7159841
23andMe allrs7159841
SNP Nexus

SNPshotrs7159841
SNPdbers7159841
MSV3drs7159841
GWAS Ctlgrs7159841
GMAF0.2971
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903294OA-icon.png]
Trait Hemostatic factors and hematological phenotypes
Title Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
Risk Allele
P-val 1.9999999999999999E-7
Odds Ratio NR NR


[PMID 17903302OA-icon.png] Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.


GET Evidence
rs7159841
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.730159
summary