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rs61761620

From SNPedia

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Make rs61761620(A;A)
Make rs61761620(A;G)
Make rs61761620(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position120889971
GeneWDR11
is asnp
is mentioned by
dbSNPrs61761620
ebirs61761620
HLIrs61761620
Exacrs61761620
Varsomers61761620
Maprs61761620
PheGenIrs61761620
hapmaprs61761620
1000 genomesrs61761620
hgdprs61761620
ensemblrs61761620
gopubmedrs61761620
geneviewrs61761620
scholarrs61761620
googlers61761620
pharmgkbrs61761620
gwascentralrs61761620
openSNPrs61761620
23andMers61761620
23andMe allrs61761620
SNP Nexus

SNPshotrs61761620
SNPdbers61761620
MSV3drs61761620
GWAS Ctlgrs61761620
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.