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rs143313688

From SNPedia

Orientationplus
Stabilizedplus
Make rs143313688(A;A)
Make rs143313688(A;G)
Make rs143313688(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position66566336
GeneCTSF
is asnp
is mentioned by
dbSNPrs143313688
dbSNP (old)rs143313688
ClinGenrs143313688
ebirs143313688
HLIrs143313688
Exacrs143313688
Varsomers143313688
Maprs143313688
PheGenIrs143313688
Biobankrs143313688
1000 genomesrs143313688
hgdprs143313688
ensemblrs143313688
gopubmedrs143313688
geneviewrs143313688
scholarrs143313688
googlers143313688
pharmgkbrs143313688
gwascentralrs143313688
openSNPrs143313688
23andMers143313688
23andMe allrs143313688
SNP Nexus

SNPshotrs143313688
SNPdbers143313688
MSV3drs143313688
GWAS Ctlgrs143313688
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.