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rs140165515

From SNPedia

Orientationplus
Stabilizedplus
Make rs140165515(A;A)
Make rs140165515(A;C)
Make rs140165515(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position109684546
GeneCCDC109B, MCUB
is asnp
is mentioned by
dbSNPrs140165515
dbSNP (old)rs140165515
ClinGenrs140165515
ebirs140165515
HLIrs140165515
Exacrs140165515
Gnomadrs140165515
Varsomers140165515
Maprs140165515
PheGenIrs140165515
Biobankrs140165515
1000 genomesrs140165515
hgdprs140165515
ensemblrs140165515
gopubmedrs140165515
geneviewrs140165515
scholarrs140165515
googlers140165515
pharmgkbrs140165515
gwascentralrs140165515
openSNPrs140165515
23andMers140165515
23andMe allrs140165515
SNP Nexus

SNPshotrs140165515
SNPdbers140165515
MSV3drs140165515
GWAS Ctlgrs140165515
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.