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rs1371799

From SNPedia

Orientationplus
Stabilizedplus
Make rs1371799(C;C)
Make rs1371799(C;T)
Make rs1371799(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position74112120
is asnp
is mentioned by
dbSNPrs1371799
ebirs1371799
HLIrs1371799
Exacrs1371799
Varsomers1371799
Maprs1371799
PheGenIrs1371799
hapmaprs1371799
1000 genomesrs1371799
hgdprs1371799
ensemblrs1371799
gopubmedrs1371799
geneviewrs1371799
scholarrs1371799
googlers1371799
pharmgkbrs1371799
gwascentralrs1371799
openSNPrs1371799
23andMers1371799
23andMe allrs1371799
SNP Nexus

SNPshotrs1371799
SNPdbers1371799
MSV3drs1371799
GWAS Ctlgrs1371799
GMAF0.466
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21738479OA-icon.png]
Trait
Title Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).
Risk Allele
P-val 2E-17
Odds Ratio None None