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rs2357013

From SNPedia

Orientationplus
Stabilizedplus
Make rs2357013(C;C)
Make rs2357013(C;T)
Make rs2357013(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position53038991
is asnp
is mentioned by
dbSNPrs2357013
ebirs2357013
HLIrs2357013
Exacrs2357013
Varsomers2357013
Maprs2357013
PheGenIrs2357013
hapmaprs2357013
1000 genomesrs2357013
hgdprs2357013
ensemblrs2357013
gopubmedrs2357013
geneviewrs2357013
scholarrs2357013
googlers2357013
pharmgkbrs2357013
gwascentralrs2357013
openSNPrs2357013
23andMers2357013
23andMe allrs2357013
SNP Nexus

SNPshotrs2357013
SNPdbers2357013
MSV3drs2357013
GWAS Ctlgrs2357013
GMAF0.3361
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


GET Evidence
rs2357013
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.677966
summary