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rs9838682

From SNPedia

Orientationplus
Stabilizedplus
Make rs9838682(A;A)
Make rs9838682(A;G)
Make rs9838682(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position30349375
GeneLOC101927995
is asnp
is mentioned by
dbSNPrs9838682
ebirs9838682
HLIrs9838682
Exacrs9838682
Varsomers9838682
Maprs9838682
PheGenIrs9838682
hapmaprs9838682
1000 genomesrs9838682
hgdprs9838682
ensemblrs9838682
gopubmedrs9838682
geneviewrs9838682
scholarrs9838682
googlers9838682
pharmgkbrs9838682
gwascentralrs9838682
openSNPrs9838682
23andMers9838682
23andMe allrs9838682
SNP Nexus

SNPshotrs9838682
SNPdbers9838682
MSV3drs9838682
GWAS Ctlgrs9838682
GMAF0.4504
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19959123OA-icon.png] Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease


[PMID 19654303OA-icon.png] Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.