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

rs6677719

From SNPedia

Orientationplus
Stabilizedplus
Make rs6677719(C;C)
Make rs6677719(C;T)
Make rs6677719(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159753330
is asnp
is mentioned by
dbSNPrs6677719
ebirs6677719
HLIrs6677719
Exacrs6677719
Varsomers6677719
Maprs6677719
PheGenIrs6677719
hapmaprs6677719
1000 genomesrs6677719
hgdprs6677719
ensemblrs6677719
gopubmedrs6677719
geneviewrs6677719
scholarrs6677719
googlers6677719
pharmgkbrs6677719
gwascentralrs6677719
openSNPrs6677719
23andMers6677719
23andMe allrs6677719
SNP Nexus

SNPshotrs6677719
SNPdbers6677719
MSV3drs6677719
GWAS Ctlgrs6677719
GMAF0.1864
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23046580] Association Study of CRP Gene polymorphism and Hypertension in Han Chinese Population