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rs7577262

From SNPedia

Orientationplus
Stabilizedplus
Make rs7577262(A;A)
Make rs7577262(A;G)
Make rs7577262(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position233910224
is asnp
is mentioned by
dbSNPrs7577262
dbSNP (classic)rs7577262
ClinGenrs7577262
ebirs7577262
HLIrs7577262
Exacrs7577262
Gnomadrs7577262
Varsomers7577262
LitVarrs7577262
Maprs7577262
PheGenIrs7577262
Biobankrs7577262
1000 genomesrs7577262
hgdprs7577262
ensemblrs7577262
geneviewrs7577262
scholarrs7577262
googlers7577262
pharmgkbrs7577262
gwascentralrs7577262
openSNPrs7577262
23andMers7577262
SNPshotrs7577262
SNPdbers7577262
MSV3drs7577262
GWAS Ctlgrs7577262
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 24165912OA-icon.png]
Trait Blood pressure measurement (cold pressor test)
Title Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.
Risk Allele A
P-val 7E-7
Odds Ratio 1.00 [0.61-1.39] mmHg decrease