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rs7844723

From SNPedia

Orientationplus
Stabilizedplus
Make rs7844723(C;C)
Make rs7844723(C;T)
Make rs7844723(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position121896264
is asnp
is mentioned by
dbSNPrs7844723
ebirs7844723
HLIrs7844723
Exacrs7844723
Varsomers7844723
Maprs7844723
PheGenIrs7844723
hapmaprs7844723
1000 genomesrs7844723
hgdprs7844723
ensemblrs7844723
gopubmedrs7844723
geneviewrs7844723
scholarrs7844723
googlers7844723
pharmgkbrs7844723
gwascentralrs7844723
openSNPrs7844723
23andMers7844723
23andMe allrs7844723
SNP Nexus

SNPshotrs7844723
SNPdbers7844723
MSV3drs7844723
GWAS Ctlgrs7844723
GMAF0.2925
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 0.0000019999999999999999
Odds Ratio NR NR


GET Evidence
rs7844723
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary