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rs188509769

From SNPedia

Orientationplus
Stabilizedplus
Make rs188509769(A;A)
Make rs188509769(A;G)
Make rs188509769(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position45940563
GenePCIF1
is asnp
is mentioned by
dbSNPrs188509769
dbSNP (old)rs188509769
ClinGenrs188509769
ebirs188509769
HLIrs188509769
Exacrs188509769
Gnomadrs188509769
Varsomers188509769
Maprs188509769
PheGenIrs188509769
Biobankrs188509769
1000 genomesrs188509769
hgdprs188509769
ensemblrs188509769
gopubmedrs188509769
geneviewrs188509769
scholarrs188509769
googlers188509769
pharmgkbrs188509769
gwascentralrs188509769
openSNPrs188509769
23andMers188509769
23andMe allrs188509769
SNP Nexus

SNPshotrs188509769
SNPdbers188509769
MSV3drs188509769
GWAS Ctlgrs188509769
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.