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rs9943849

From SNPedia

Orientationplus
Stabilizedplus
Make rs9943849(C;C)
Make rs9943849(C;T)
Make rs9943849(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position68976976
is asnp
is mentioned by
dbSNPrs9943849
ebirs9943849
HLIrs9943849
Exacrs9943849
Varsomers9943849
Maprs9943849
PheGenIrs9943849
hapmaprs9943849
1000 genomesrs9943849
hgdprs9943849
ensemblrs9943849
gopubmedrs9943849
geneviewrs9943849
scholarrs9943849
googlers9943849
pharmgkbrs9943849
gwascentralrs9943849
openSNPrs9943849
23andMers9943849
23andMe allrs9943849
SNP Nexus

SNPshotrs9943849
SNPdbers9943849
MSV3drs9943849
GWAS Ctlgrs9943849
GMAF0.2406
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20673876] Genome-Wide Association-, Replication-, and Neuroimaging Study Implicates HOMER1 in the Etiology of Major Depression