Have questions? Visit https://www.reddit.com/r/SNPedia

rs111596332

From SNPedia

Orientationplus
Stabilizedplus
Make rs111596332(A;A)
Make rs111596332(A;G)
Make rs111596332(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position31476659
GeneDEFB124, REM1
is asnp
is mentioned by
dbSNPrs111596332
dbSNP (old)rs111596332
ClinGenrs111596332
ebirs111596332
HLIrs111596332
Exacrs111596332
Varsomers111596332
Maprs111596332
PheGenIrs111596332
Biobankrs111596332
1000 genomesrs111596332
hgdprs111596332
ensemblrs111596332
gopubmedrs111596332
geneviewrs111596332
scholarrs111596332
googlers111596332
pharmgkbrs111596332
gwascentralrs111596332
openSNPrs111596332
23andMers111596332
23andMe allrs111596332
SNP Nexus

SNPshotrs111596332
SNPdbers111596332
MSV3drs111596332
GWAS Ctlgrs111596332
Max Magnitude
[PMID 27120077] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.