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rs148322402

From SNPedia

Orientationplus
Stabilizedplus
Make rs148322402(A;A)
Make rs148322402(A;G)
Make rs148322402(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position102070411
GeneCUX1
is asnp
is mentioned by
dbSNPrs148322402
dbSNP (old)rs148322402
ClinGenrs148322402
ebirs148322402
HLIrs148322402
Exacrs148322402
Gnomadrs148322402
Varsomers148322402
Maprs148322402
PheGenIrs148322402
Biobankrs148322402
1000 genomesrs148322402
hgdprs148322402
ensemblrs148322402
gopubmedrs148322402
geneviewrs148322402
scholarrs148322402
googlers148322402
pharmgkbrs148322402
gwascentralrs148322402
openSNPrs148322402
23andMers148322402
23andMe allrs148322402
SNP Nexus

SNPshotrs148322402
SNPdbers148322402
MSV3drs148322402
GWAS Ctlgrs148322402
Max Magnitude
[PMID 27120077OA-icon.png] 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.