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rs10956483

From SNPedia

Orientationplus
Stabilizedplus
Make rs10956483(C;C)
Make rs10956483(C;G)
Make rs10956483(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position129559864
is asnp
is mentioned by
dbSNPrs10956483
ebirs10956483
HLIrs10956483
Exacrs10956483
Varsomers10956483
Maprs10956483
PheGenIrs10956483
hapmaprs10956483
1000 genomesrs10956483
hgdprs10956483
ensemblrs10956483
gopubmedrs10956483
geneviewrs10956483
scholarrs10956483
googlers10956483
pharmgkbrs10956483
gwascentralrs10956483
openSNPrs10956483
23andMers10956483
23andMe allrs10956483
SNP Nexus

SNPshotrs10956483
SNPdbers10956483
MSV3drs10956483
GWAS Ctlgrs10956483
GMAF0.2466
Max Magnitude
? (C;C) (C;G) (G;G) 28
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 C
P-val 2E-10
Odds Ratio 0.0710 [0.05-0.09] unit increase