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rs828199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs828199(C;T)
Make rs828199(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position90718584
is asnp
is mentioned by
dbSNPrs828199
ebirs828199
HLIrs828199
Exacrs828199
Varsomers828199
Maprs828199
PheGenIrs828199
hapmaprs828199
1000 genomesrs828199
hgdprs828199
ensemblrs828199
gopubmedrs828199
geneviewrs828199
scholarrs828199
googlers828199
pharmgkbrs828199
gwascentralrs828199
openSNPrs828199
23andMers828199
23andMe allrs828199
SNP Nexus

SNPshotrs828199
SNPdbers828199
MSV3drs828199
GWAS Ctlgrs828199
Merged fromRs1616905
GMAF0.01882
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 20863575] Lack of association between response of OROS-methylphenidate and norepinephrine transporter (SLC6A2) polymorphism in Korean ADHD.