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rs11169282

From SNPedia
Orientationplus
Stabilizedplus
Make rs11169282(A;A)
Make rs11169282(A;G)
Make rs11169282(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position50136188
GeneCERS5
is asnp
is mentioned by
dbSNPrs11169282
dbSNP (old)rs11169282
ClinGenrs11169282
ebirs11169282
HLIrs11169282
Exacrs11169282
Gnomadrs11169282
Varsomers11169282
Maprs11169282
PheGenIrs11169282
Biobankrs11169282
1000 genomesrs11169282
hgdprs11169282
ensemblrs11169282
gopubmedrs11169282
geneviewrs11169282
scholarrs11169282
googlers11169282
pharmgkbrs11169282
gwascentralrs11169282
openSNPrs11169282
23andMers11169282
23andMe allrs11169282
SNPshotrs11169282
SNPdbers11169282
MSV3drs11169282
GWAS Ctlgrs11169282
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 29500710] Genome-wide genotype-based risk model for survival in core binding factor acute myeloid leukemia patients.