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rs3766680

From SNPedia

Orientationminus
Stabilizedminus
Make rs3766680(A;A)
Make rs3766680(A;G)
Make rs3766680(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position175327312
GeneTNR
is asnp
is mentioned by
dbSNPrs3766680
ebirs3766680
HLIrs3766680
Exacrs3766680
Varsomers3766680
Maprs3766680
PheGenIrs3766680
hapmaprs3766680
1000 genomesrs3766680
hgdprs3766680
ensemblrs3766680
gopubmedrs3766680
geneviewrs3766680
scholarrs3766680
googlers3766680
pharmgkbrs3766680
gwascentralrs3766680
openSNPrs3766680
23andMers3766680
23andMe allrs3766680
SNP Nexus

SNPshotrs3766680
SNPdbers3766680
MSV3drs3766680
GWAS Ctlgrs3766680
GMAF0.4578
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903302OA-icon.png]
Trait Tonometry
Title Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Risk Allele
P-val 0.0000039999999999999998
Odds Ratio NR NR


GET Evidence
rs3766680
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.570312
summary