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rs10980800

From SNPedia

Orientationplus
Stabilizedplus
Make rs10980800(C;C)
Make rs10980800(C;T)
Make rs10980800(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position111153625
is asnp
is mentioned by
dbSNPrs10980800
ebirs10980800
HLIrs10980800
Exacrs10980800
Varsomers10980800
Maprs10980800
PheGenIrs10980800
hapmaprs10980800
1000 genomesrs10980800
hgdprs10980800
ensemblrs10980800
gopubmedrs10980800
geneviewrs10980800
scholarrs10980800
googlers10980800
pharmgkbrs10980800
gwascentralrs10980800
openSNPrs10980800
23andMers10980800
23andMe allrs10980800
SNP Nexus

SNPshotrs10980800
SNPdbers10980800
MSV3drs10980800
GWAS Ctlgrs10980800
Max Magnitude
? (C;C) (C;T) (T;T) 28
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-22
Odds Ratio .04 [0.034-0.050] unit decrease