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rs375954692

From SNPedia

Orientationplus
Stabilizedplus
Make rs375954692(C;C)
Make rs375954692(C;T)
Make rs375954692(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position1250169
GeneMUC5B
is asnp
is mentioned by
dbSNPrs375954692
dbSNP (old)rs375954692
ClinGenrs375954692
ebirs375954692
HLIrs375954692
Exacrs375954692
Varsomers375954692
Maprs375954692
PheGenIrs375954692
Biobankrs375954692
1000 genomesrs375954692
hgdprs375954692
ensemblrs375954692
gopubmedrs375954692
geneviewrs375954692
scholarrs375954692
googlers375954692
pharmgkbrs375954692
gwascentralrs375954692
openSNPrs375954692
23andMers375954692
23andMe allrs375954692
SNP Nexus

SNPshotrs375954692
SNPdbers375954692
MSV3drs375954692
GWAS Ctlgrs375954692
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.