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rs148209474

From SNPedia

Orientationplus
Stabilizedplus
Make rs148209474(C;C)
Make rs148209474(C;T)
Make rs148209474(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position66668863
GeneRBM4, RBM4B
is asnp
is mentioned by
dbSNPrs148209474
dbSNP (old)rs148209474
ClinGenrs148209474
ebirs148209474
HLIrs148209474
Exacrs148209474
Gnomadrs148209474
Varsomers148209474
Maprs148209474
PheGenIrs148209474
Biobankrs148209474
1000 genomesrs148209474
hgdprs148209474
ensemblrs148209474
gopubmedrs148209474
geneviewrs148209474
scholarrs148209474
googlers148209474
pharmgkbrs148209474
gwascentralrs148209474
openSNPrs148209474
23andMers148209474
23andMe allrs148209474
SNP Nexus

SNPshotrs148209474
SNPdbers148209474
MSV3drs148209474
GWAS Ctlgrs148209474
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.