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rs636864

From SNPedia

Orientationplus
Stabilizedplus
Make rs636864(C;C)
Make rs636864(C;T)
Make rs636864(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position149204470
is asnp
is mentioned by
dbSNPrs636864
ebirs636864
HLIrs636864
Exacrs636864
Varsomers636864
Maprs636864
PheGenIrs636864
hapmaprs636864
1000 genomesrs636864
hgdprs636864
ensemblrs636864
gopubmedrs636864
geneviewrs636864
scholarrs636864
googlers636864
pharmgkbrs636864
gwascentralrs636864
openSNPrs636864
23andMers636864
23andMe allrs636864
SNP Nexus

SNPshotrs636864
SNPdbers636864
MSV3drs636864
GWAS Ctlgrs636864
GMAF0.2617
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 17903302OA-icon.png] diastolic blood pressure


GET Evidence
rs636864
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.320312
summary