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rs1397048

From SNPedia

Orientationminus
Stabilizedminus
Make rs1397048(A;A)
Make rs1397048(A;G)
Make rs1397048(G;G)
ReferenceGRCh37 37.1/131
Chromosome11
Position56466099
GeneOR9G1
is asnp
is mentioned by
dbSNPrs1397048
ebirs1397048
HLIrs1397048
Exacrs1397048
Varsomers1397048
Maprs1397048
PheGenIrs1397048
hapmaprs1397048
1000 genomesrs1397048
hgdprs1397048
ensemblrs1397048
gopubmedrs1397048
geneviewrs1397048
scholarrs1397048
googlers1397048
pharmgkbrs1397048
gwascentralrs1397048
openSNPrs1397048
23andMers1397048
23andMe allrs1397048
SNP Nexus

SNPshotrs1397048
SNPdbers1397048
MSV3drs1397048
GWAS Ctlgrs1397048
GMAF0.466
Max Magnitude
? (A;A) (A;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 7.0000000000000005E-8
Odds Ratio NR NR


[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


GET Evidence
rs1397048
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507936
summary