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rs8078723

From SNPedia

Orientationplus
Stabilizedplus
Make rs8078723(C;C)
Make rs8078723(C;T)
Make rs8078723(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position40010626
is asnp
is mentioned by
dbSNPrs8078723
ebirs8078723
HLIrs8078723
Exacrs8078723
Varsomers8078723
Maprs8078723
PheGenIrs8078723
hapmaprs8078723
1000 genomesrs8078723
hgdprs8078723
ensemblrs8078723
gopubmedrs8078723
geneviewrs8078723
scholarrs8078723
googlers8078723
pharmgkbrs8078723
gwascentralrs8078723
openSNPrs8078723
23andMers8078723
23andMe allrs8078723
SNP Nexus

SNPshotrs8078723
SNPdbers8078723
MSV3drs8078723
GWAS Ctlgrs8078723
GMAF0.3673
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22788528] Genetic associations with C-reactive protein level and white blood cell count in the KARE study


[PMID 19408013OA-icon.png] Strategies and issues in the detection of pathway enrichment in genome-wide association studies.

GWAS snp
PMID [PMID 21738480OA-icon.png]
Trait White blood cell count
Title Multiple loci are associated with white blood cell phenotypes.
Risk Allele T
P-val 2E-31
Odds Ratio .04 [0.034-0.048] unit decrease