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rs17061085

From SNPedia

Orientationplus
Stabilizedplus
Make rs17061085(A;A)
Make rs17061085(A;G)
Make rs17061085(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position59705999
is asnp
is mentioned by
dbSNPrs17061085
ebirs17061085
HLIrs17061085
Exacrs17061085
Varsomers17061085
Maprs17061085
PheGenIrs17061085
hapmaprs17061085
1000 genomesrs17061085
hgdprs17061085
ensemblrs17061085
gopubmedrs17061085
geneviewrs17061085
scholarrs17061085
googlers17061085
pharmgkbrs17061085
gwascentralrs17061085
openSNPrs17061085
23andMers17061085
23andMe allrs17061085
SNP Nexus

SNPshotrs17061085
SNPdbers17061085
MSV3drs17061085
GWAS Ctlgrs17061085
GMAF0.09642
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