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rs6785358

From SNPedia

Orientationplus
Stabilizedplus
Make rs6785358(A;A)
Make rs6785358(A;G)
Make rs6785358(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position30602723
is asnp
is mentioned by
dbSNPrs6785358
ebirs6785358
HLIrs6785358
Exacrs6785358
Varsomers6785358
Maprs6785358
PheGenIrs6785358
hapmaprs6785358
1000 genomesrs6785358
hgdprs6785358
ensemblrs6785358
gopubmedrs6785358
geneviewrs6785358
scholarrs6785358
googlers6785358
pharmgkbrs6785358
gwascentralrs6785358
openSNPrs6785358
23andMers6785358
23andMe allrs6785358
SNP Nexus

SNPshotrs6785358
SNPdbers6785358
MSV3drs6785358
GWAS Ctlgrs6785358
GMAF0.1552
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 23157888] [An association study between transforming growth factor-β1 receptor 2 gene polymorphisms and essential hypertension]


[PMID 26022443] Association of TGFBR2 rs6785358 Polymorphism with Increased Risk of Congenital Ventricular Septal Defect in a Chinese Population