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

rs3821396

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs3821396(C;T)
Make rs3821396(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position21664877
GeneZNF385D
is asnp
is mentioned by
dbSNPrs3821396
ebirs3821396
HLIrs3821396
Exacrs3821396
Varsomers3821396
Maprs3821396
PheGenIrs3821396
hapmaprs3821396
1000 genomesrs3821396
hgdprs3821396
ensemblrs3821396
gopubmedrs3821396
geneviewrs3821396
scholarrs3821396
googlers3821396
pharmgkbrs3821396
gwascentralrs3821396
openSNPrs3821396
23andMers3821396
23andMe allrs3821396
SNP Nexus

SNPshotrs3821396
SNPdbers3821396
MSV3drs3821396
GWAS Ctlgrs3821396
GMAF0.1143
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18711365OA-icon.png]
Trait Bipolar disorder
Title Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Risk Allele A
P-val 0.0000050000000000000004
Odds Ratio 1.23 [NR]


GET Evidence
rs3821396
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0832869
summary