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rs1200821

From SNPedia

Orientationminus
Stabilizedminus
Make rs1200821(C;C)
Make rs1200821(C;T)
Make rs1200821(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position37270652
is asnp
is mentioned by
dbSNPrs1200821
ebirs1200821
HLIrs1200821
Exacrs1200821
Varsomers1200821
Maprs1200821
PheGenIrs1200821
hapmaprs1200821
1000 genomesrs1200821
hgdprs1200821
ensemblrs1200821
gopubmedrs1200821
geneviewrs1200821
scholarrs1200821
googlers1200821
pharmgkbrs1200821
gwascentralrs1200821
openSNPrs1200821
23andMers1200821
23andMe allrs1200821
SNP Nexus

SNPshotrs1200821
SNPdbers1200821
MSV3drs1200821
GWAS Ctlgrs1200821
GMAF0.477
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 0.0000060000000000000002
Odds Ratio NR NR

[PMID 17903301OA-icon.png] Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.


GET Evidence
rs1200821
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.523438
summary