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rs144288263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144288263(A;A)
Make rs144288263(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position27787965
GeneESCO2
is asnp
is mentioned by
dbSNPrs144288263
ClinGenrs144288263
ebirs144288263
HLIrs144288263
Exacrs144288263
Varsomers144288263
Maprs144288263
PheGenIrs144288263
hapmaprs144288263
1000 genomesrs144288263
hgdprs144288263
ensemblrs144288263
gopubmedrs144288263
geneviewrs144288263
scholarrs144288263
googlers144288263
pharmgkbrs144288263
gwascentralrs144288263
openSNPrs144288263
23andMers144288263
23andMe allrs144288263
SNP Nexus

SNPshotrs144288263
SNPdbers144288263
MSV3drs144288263
GWAS Ctlgrs144288263
Max Magnitude0
[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.
ClinVar
Risk rs144288263(A;A)
Alt rs144288263(A;A)
Reference Rs144288263(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ESCO2
CLNDBN not specified
Reversed 0
HGVS NC_000008.10:g.27645482G>A
CLNSRC
CLNACC RCV000395189.1,