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rs143573515

From SNPedia

Orientationplus
Stabilizedplus
Make rs143573515(C;C)
Make rs143573515(C;T)
Make rs143573515(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position49531818
GeneDAG1
is asnp
is mentioned by
dbSNPrs143573515
dbSNP (old)rs143573515
ClinGenrs143573515
ebirs143573515
HLIrs143573515
Exacrs143573515
Gnomadrs143573515
Varsomers143573515
Maprs143573515
PheGenIrs143573515
Biobankrs143573515
1000 genomesrs143573515
hgdprs143573515
ensemblrs143573515
gopubmedrs143573515
geneviewrs143573515
scholarrs143573515
googlers143573515
pharmgkbrs143573515
gwascentralrs143573515
openSNPrs143573515
23andMers143573515
23andMe allrs143573515
SNP Nexus

SNPshotrs143573515
SNPdbers143573515
MSV3drs143573515
GWAS Ctlgrs143573515
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.
ClinVar
Risk rs143573515(T;T)
Alt rs143573515(T;T)
Reference rs143573515(C;C)
Significance Unknown
Disease not specified
Variation info
Gene DAG1
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.49569251C>T
CLNSRC
CLNACC RCV000373932.1,