Have questions? Visit https://www.reddit.com/r/SNPedia

rs6904416

From SNPedia

Orientationplus
Stabilizedplus
Make rs6904416(C;C)
Make rs6904416(C;T)
Make rs6904416(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position98542613
is asnp
is mentioned by
dbSNPrs6904416
dbSNP (classic)rs6904416
ClinGenrs6904416
ebirs6904416
HLIrs6904416
Exacrs6904416
Gnomadrs6904416
Varsomers6904416
LitVarrs6904416
Maprs6904416
PheGenIrs6904416
Biobankrs6904416
1000 genomesrs6904416
hgdprs6904416
ensemblrs6904416
geneviewrs6904416
scholarrs6904416
googlers6904416
pharmgkbrs6904416
gwascentralrs6904416
openSNPrs6904416
23andMers6904416
SNPshotrs6904416
SNPdbers6904416
MSV3drs6904416
GWAS Ctlgrs6904416
GMAF0.08127
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22788528]
Trait C-reactive protein and white blood cell count
Title Genetic associations with C-reactive protein level and white blood cell count in the KARE study.
Risk Allele C
P-val 9E-10
Odds Ratio .18 [NR] mg/dl increase