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

rs139995395

From SNPedia

Orientationplus
Stabilizedplus
Make rs139995395(C;C)
Make rs139995395(C;T)
Make rs139995395(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position67947367
GeneSLC12A4
is asnp
is mentioned by
dbSNPrs139995395
dbSNP (old)rs139995395
ClinGenrs139995395
ebirs139995395
HLIrs139995395
Exacrs139995395
Gnomadrs139995395
Varsomers139995395
Maprs139995395
PheGenIrs139995395
Biobankrs139995395
1000 genomesrs139995395
hgdprs139995395
ensemblrs139995395
gopubmedrs139995395
geneviewrs139995395
scholarrs139995395
googlers139995395
pharmgkbrs139995395
gwascentralrs139995395
openSNPrs139995395
23andMers139995395
23andMe allrs139995395
SNP Nexus

SNPshotrs139995395
SNPdbers139995395
MSV3drs139995395
GWAS Ctlgrs139995395
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.