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rs182714476

From SNPedia

Orientationplus
Stabilizedplus
Make rs182714476(A;A)
Make rs182714476(A;G)
Make rs182714476(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position228377508
GeneOBSCN
is asnp
is mentioned by
dbSNPrs182714476
dbSNP (old)rs182714476
ClinGenrs182714476
ebirs182714476
HLIrs182714476
Exacrs182714476
Gnomadrs182714476
Varsomers182714476
Maprs182714476
PheGenIrs182714476
Biobankrs182714476
1000 genomesrs182714476
hgdprs182714476
ensemblrs182714476
gopubmedrs182714476
geneviewrs182714476
scholarrs182714476
googlers182714476
pharmgkbrs182714476
gwascentralrs182714476
openSNPrs182714476
23andMers182714476
23andMe allrs182714476
SNP Nexus

SNPshotrs182714476
SNPdbers182714476
MSV3drs182714476
GWAS Ctlgrs182714476
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.