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

rs138745887

From SNPedia

Orientationplus
Stabilizedplus
Make rs138745887(C;C)
Make rs138745887(C;T)
Make rs138745887(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position121940930
GeneSLC15A2
is asnp
is mentioned by
dbSNPrs138745887
dbSNP (old)rs138745887
ClinGenrs138745887
ebirs138745887
HLIrs138745887
Exacrs138745887
Gnomadrs138745887
Varsomers138745887
Maprs138745887
PheGenIrs138745887
Biobankrs138745887
1000 genomesrs138745887
hgdprs138745887
ensemblrs138745887
gopubmedrs138745887
geneviewrs138745887
scholarrs138745887
googlers138745887
pharmgkbrs138745887
gwascentralrs138745887
openSNPrs138745887
23andMers138745887
23andMe allrs138745887
SNP Nexus

SNPshotrs138745887
SNPdbers138745887
MSV3drs138745887
GWAS Ctlgrs138745887
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.