Have questions? Visit https://www.reddit.com/r/SNPedia

rs78259398

From SNPedia

Orientationplus
Make rs78259398(C;C)
Make rs78259398(C;T)
Make rs78259398(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position41778035
GeneVWA8
is asnp
is mentioned by
dbSNPrs78259398
ebirs78259398
HLIrs78259398
Exacrs78259398
Varsomers78259398
Maprs78259398
PheGenIrs78259398
hapmaprs78259398
1000 genomesrs78259398
hgdprs78259398
ensemblrs78259398
gopubmedrs78259398
geneviewrs78259398
scholarrs78259398
googlers78259398
pharmgkbrs78259398
gwascentralrs78259398
openSNPrs78259398
23andMers78259398
23andMe allrs78259398
SNP Nexus

SNPshotrs78259398
SNPdbers78259398
MSV3drs78259398
GWAS Ctlgrs78259398
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.