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rs150218881

From SNPedia

Orientationplus
Stabilizedplus
Make rs150218881(C;C)
Make rs150218881(C;T)
Make rs150218881(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position19132036
GeneDGCR14, TSSK2
is asnp
is mentioned by
dbSNPrs150218881
dbSNP (old)rs150218881
ClinGenrs150218881
ebirs150218881
HLIrs150218881
Exacrs150218881
Gnomadrs150218881
Varsomers150218881
Maprs150218881
PheGenIrs150218881
Biobankrs150218881
1000 genomesrs150218881
hgdprs150218881
ensemblrs150218881
gopubmedrs150218881
geneviewrs150218881
scholarrs150218881
googlers150218881
pharmgkbrs150218881
gwascentralrs150218881
openSNPrs150218881
23andMers150218881
23andMe allrs150218881
SNP Nexus

SNPshotrs150218881
SNPdbers150218881
MSV3drs150218881
GWAS Ctlgrs150218881
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.