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rs199962136

From SNPedia

Orientationplus
Stabilizedplus
Make rs199962136(A;A)
Make rs199962136(A;G)
Make rs199962136(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position119052704
GeneHYOU1
is asnp
is mentioned by
dbSNPrs199962136
dbSNP (old)rs199962136
ClinGenrs199962136
ebirs199962136
HLIrs199962136
Exacrs199962136
Gnomadrs199962136
Varsomers199962136
Maprs199962136
PheGenIrs199962136
Biobankrs199962136
1000 genomesrs199962136
hgdprs199962136
ensemblrs199962136
gopubmedrs199962136
geneviewrs199962136
scholarrs199962136
googlers199962136
pharmgkbrs199962136
gwascentralrs199962136
openSNPrs199962136
23andMers199962136
23andMe allrs199962136
SNP Nexus

SNPshotrs199962136
SNPdbers199962136
MSV3drs199962136
GWAS Ctlgrs199962136
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.