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rs4794822

From SNPedia

Orientationplus
Stabilizedplus
Make rs4794822(C;C)
Make rs4794822(C;T)
Make rs4794822(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position40000459
is asnp
is mentioned by
dbSNPrs4794822
ebirs4794822
HLIrs4794822
Exacrs4794822
Varsomers4794822
Maprs4794822
PheGenIrs4794822
hapmaprs4794822
1000 genomesrs4794822
hgdprs4794822
ensemblrs4794822
gopubmedrs4794822
geneviewrs4794822
scholarrs4794822
googlers4794822
pharmgkbrs4794822
gwascentralrs4794822
openSNPrs4794822
23andMers4794822
23andMe allrs4794822
SNP Nexus

SNPshotrs4794822
SNPdbers4794822
MSV3drs4794822
GWAS Ctlgrs4794822
GMAF0.3705
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20172861]
Trait Neutrophil count
Title Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count.
Risk Allele C
P-val 6E-10
Odds Ratio 0.10 [0.07-0.13] unit decrease in log(neutrophil ct)
GWAS snp
PMID [PMID 21738478OA-icon.png]
Trait
Title Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population.
Risk Allele T
P-val 4E-16
Odds Ratio 0.0930 [0.07-0.11] unit increase
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 9E-35
Odds Ratio .02 [0.018-0.025] unit increase