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rs565229

From SNPedia

Orientationminus
Stabilizedminus
Make rs565229(C;C)
Make rs565229(C;T)
Make rs565229(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position122318757
GeneLOC100507145
is asnp
is mentioned by
dbSNPrs565229
ebirs565229
HLIrs565229
Exacrs565229
Varsomers565229
Maprs565229
PheGenIrs565229
hapmaprs565229
1000 genomesrs565229
hgdprs565229
ensemblrs565229
gopubmedrs565229
geneviewrs565229
scholarrs565229
googlers565229
pharmgkbrs565229
gwascentralrs565229
openSNPrs565229
23andMers565229
23andMe allrs565229
SNP Nexus

SNPshotrs565229
SNPdbers565229
MSV3drs565229
GWAS Ctlgrs565229
GMAF0.1612
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 0.0000039999999999999998
Odds Ratio NR NR


GET Evidence
rs565229
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.15625
summary