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rs1160297

From SNPedia

Orientationplus
Stabilizedplus
Make rs1160297(C;C)
Make rs1160297(C;G)
Make rs1160297(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position53010182
is asnp
is mentioned by
dbSNPrs1160297
ebirs1160297
HLIrs1160297
Exacrs1160297
Varsomers1160297
Maprs1160297
PheGenIrs1160297
hapmaprs1160297
1000 genomesrs1160297
hgdprs1160297
ensemblrs1160297
gopubmedrs1160297
geneviewrs1160297
scholarrs1160297
googlers1160297
pharmgkbrs1160297
gwascentralrs1160297
openSNPrs1160297
23andMers1160297
23andMe allrs1160297
SNP Nexus

SNPshotrs1160297
SNPdbers1160297
MSV3drs1160297
GWAS Ctlgrs1160297
GMAF0.3425
Max Magnitude
? (C;C) (C;G) (G;G) 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 9.9999999999999995E-7
Odds Ratio NR NR


GET Evidence
rs1160297
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.671875
summary