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rs148547886

From SNPedia

Orientationplus
Stabilizedplus
Make rs148547886(A;A)
Make rs148547886(A;G)
Make rs148547886(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position105066654
GeneALDH1L2
is asnp
is mentioned by
dbSNPrs148547886
dbSNP (old)rs148547886
ClinGenrs148547886
ebirs148547886
HLIrs148547886
Exacrs148547886
Varsomers148547886
Maprs148547886
PheGenIrs148547886
Biobankrs148547886
1000 genomesrs148547886
hgdprs148547886
ensemblrs148547886
gopubmedrs148547886
geneviewrs148547886
scholarrs148547886
googlers148547886
pharmgkbrs148547886
gwascentralrs148547886
openSNPrs148547886
23andMers148547886
23andMe allrs148547886
SNP Nexus

SNPshotrs148547886
SNPdbers148547886
MSV3drs148547886
GWAS Ctlgrs148547886
Max Magnitude
[PMID 27120077] 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.