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rs3773643

From SNPedia

Orientationplus
Stabilizedplus
Make rs3773643(A;A)
Make rs3773643(A;G)
Make rs3773643(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position30668751
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs3773643
ebirs3773643
HLIrs3773643
Exacrs3773643
Varsomers3773643
Maprs3773643
PheGenIrs3773643
hapmaprs3773643
1000 genomesrs3773643
hgdprs3773643
ensemblrs3773643
gopubmedrs3773643
geneviewrs3773643
scholarrs3773643
googlers3773643
pharmgkbrs3773643
gwascentralrs3773643
openSNPrs3773643
23andMers3773643
23andMe allrs3773643
SNP Nexus

SNPshotrs3773643
SNPdbers3773643
MSV3drs3773643
GWAS Ctlgrs3773643
GMAF0.1837
Max Magnitude
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 1.9999999999999999E-7
Odds Ratio NR NR


GET Evidence
rs3773643
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.193548
summary