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rs2527866

From SNPedia

Orientationminus
Stabilizedminus
Make rs2527866(G;G)
Make rs2527866(G;T)
Make rs2527866(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position157297602
is asnp
is mentioned by
dbSNPrs2527866
ebirs2527866
HLIrs2527866
Exacrs2527866
Varsomers2527866
Maprs2527866
PheGenIrs2527866
hapmaprs2527866
1000 genomesrs2527866
hgdprs2527866
ensemblrs2527866
gopubmedrs2527866
geneviewrs2527866
scholarrs2527866
googlers2527866
pharmgkbrs2527866
gwascentralrs2527866
openSNPrs2527866
23andMers2527866
23andMe allrs2527866
SNP Nexus

SNPshotrs2527866
SNPdbers2527866
MSV3drs2527866
GWAS Ctlgrs2527866
GMAF0.4293
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele C
P-val 0.000003
Odds Ratio 0.27 [NR] mm Hg decrease

systolic blood pressure being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs2527866
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.414062
summary