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

rs375533918

From SNPedia

Orientationplus
Stabilizedplus
Make rs375533918(A;A)
Make rs375533918(A;T)
Make rs375533918(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position36280753
GeneCOMMD9
is asnp
is mentioned by
dbSNPrs375533918
dbSNP (old)rs375533918
ClinGenrs375533918
ebirs375533918
HLIrs375533918
Exacrs375533918
Gnomadrs375533918
Varsomers375533918
Maprs375533918
PheGenIrs375533918
Biobankrs375533918
1000 genomesrs375533918
hgdprs375533918
ensemblrs375533918
gopubmedrs375533918
geneviewrs375533918
scholarrs375533918
googlers375533918
pharmgkbrs375533918
gwascentralrs375533918
openSNPrs375533918
23andMers375533918
23andMe allrs375533918
SNP Nexus

SNPshotrs375533918
SNPdbers375533918
MSV3drs375533918
GWAS Ctlgrs375533918
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.