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rs9949006

From SNPedia

Orientationplus
Stabilizedplus
Make rs9949006(A;A)
Make rs9949006(A;G)
Make rs9949006(G;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position1916607
GeneLOC105371958
is asnp
is mentioned by
dbSNPrs9949006
dbSNP (old)rs9949006
ClinGenrs9949006
ebirs9949006
HLIrs9949006
Exacrs9949006
Varsomers9949006
Maprs9949006
PheGenIrs9949006
Biobankrs9949006
1000 genomesrs9949006
hgdprs9949006
ensemblrs9949006
gopubmedrs9949006
geneviewrs9949006
scholarrs9949006
googlers9949006
pharmgkbrs9949006
gwascentralrs9949006
openSNPrs9949006
23andMers9949006
23andMe allrs9949006
SNP Nexus

SNPshotrs9949006
SNPdbers9949006
MSV3drs9949006
GWAS Ctlgrs9949006
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 25875332OA-icon.png] Genome-Wide Analysis of Attention Deficit Hyperactivity Disorder in Norway