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rs200223984

From SNPedia

Orientationplus
Stabilizedplus
Make rs200223984(A;A)
Make rs200223984(A;C)
Make rs200223984(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position102139377
GeneHSP90AA1, WDR20
is asnp
is mentioned by
dbSNPrs200223984
dbSNP (old)rs200223984
ClinGenrs200223984
ebirs200223984
HLIrs200223984
Exacrs200223984
Varsomers200223984
Maprs200223984
PheGenIrs200223984
Biobankrs200223984
1000 genomesrs200223984
hgdprs200223984
ensemblrs200223984
gopubmedrs200223984
geneviewrs200223984
scholarrs200223984
googlers200223984
pharmgkbrs200223984
gwascentralrs200223984
openSNPrs200223984
23andMers200223984
23andMe allrs200223984
SNP Nexus

SNPshotrs200223984
SNPdbers200223984
MSV3drs200223984
GWAS Ctlgrs200223984
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.