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rs17691914

From SNPedia

Orientationplus
Stabilizedplus
Make rs17691914(A;A)
Make rs17691914(A;G)
Make rs17691914(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position34921311
GeneLOC101928135
is asnp
is mentioned by
dbSNPrs17691914
ebirs17691914
HLIrs17691914
Exacrs17691914
Varsomers17691914
Maprs17691914
PheGenIrs17691914
hapmaprs17691914
1000 genomesrs17691914
hgdprs17691914
ensemblrs17691914
gopubmedrs17691914
geneviewrs17691914
scholarrs17691914
googlers17691914
pharmgkbrs17691914
gwascentralrs17691914
openSNPrs17691914
23andMers17691914
23andMe allrs17691914
SNP Nexus

SNPshotrs17691914
SNPdbers17691914
MSV3drs17691914
GWAS Ctlgrs17691914
GMAF0.06749
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21980348OA-icon.png] Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgery