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

rs4262150

From SNPedia

Orientationplus
Stabilizedplus
Make rs4262150(G;G)
Make rs4262150(G;T)
Make rs4262150(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position152908893
GeneLINC01470
is asnp
is mentioned by
dbSNPrs4262150
dbSNP (classic)rs4262150
ClinGenrs4262150
ebirs4262150
HLIrs4262150
Exacrs4262150
Gnomadrs4262150
Varsomers4262150
LitVarrs4262150
Maprs4262150
PheGenIrs4262150
Biobankrs4262150
1000 genomesrs4262150
hgdprs4262150
ensemblrs4262150
geneviewrs4262150
scholarrs4262150
googlers4262150
pharmgkbrs4262150
gwascentralrs4262150
openSNPrs4262150
23andMers4262150
SNPshotrs4262150
SNPdbers4262150
MSV3drs4262150
GWAS Ctlgrs4262150
GMAF0.3154
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 22688191OA-icon.png]
Trait
Title Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Risk Allele
P-val 0.000007
Odds Ratio 1.2200 None