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rs225717

From SNPedia

Orientationplus
Stabilizedplus
Make rs225717(C;C)
Make rs225717(C;T)
Make rs225717(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position142226962
is asnp
is mentioned by
dbSNPrs225717
ebirs225717
HLIrs225717
Exacrs225717
Varsomers225717
Maprs225717
PheGenIrs225717
hapmaprs225717
1000 genomesrs225717
hgdprs225717
ensemblrs225717
gopubmedrs225717
geneviewrs225717
scholarrs225717
googlers225717
pharmgkbrs225717
gwascentralrs225717
openSNPrs225717
23andMers225717
23andMe allrs225717
SNP Nexus

SNPshotrs225717
SNPdbers225717
MSV3drs225717
GWAS Ctlgrs225717
GMAF0.1538
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21060863OA-icon.png]
Trait
Title Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Risk Allele C
P-val 1E-16
Odds Ratio 1.9000 [1.45-2.35] um decrease