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rs139106853

From SNPedia

Orientationplus
Stabilizedplus
Make rs139106853(A;A)
Make rs139106853(A;G)
Make rs139106853(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position105189823
GeneAPPL2
is asnp
is mentioned by
dbSNPrs139106853
dbSNP (old)rs139106853
ClinGenrs139106853
ebirs139106853
HLIrs139106853
Exacrs139106853
Varsomers139106853
Maprs139106853
PheGenIrs139106853
Biobankrs139106853
1000 genomesrs139106853
hgdprs139106853
ensemblrs139106853
gopubmedrs139106853
geneviewrs139106853
scholarrs139106853
googlers139106853
pharmgkbrs139106853
gwascentralrs139106853
openSNPrs139106853
23andMers139106853
23andMe allrs139106853
SNP Nexus

SNPshotrs139106853
SNPdbers139106853
MSV3drs139106853
GWAS Ctlgrs139106853
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.