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rs4996815

From SNPedia

Orientationplus
Stabilizedplus
Make rs4996815(G;G)
Make rs4996815(G;T)
Make rs4996815(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position105999312
is asnp
is mentioned by
dbSNPrs4996815
dbSNP (classic)rs4996815
ClinGenrs4996815
ebirs4996815
HLIrs4996815
Exacrs4996815
Gnomadrs4996815
Varsomers4996815
LitVarrs4996815
Maprs4996815
PheGenIrs4996815
Biobankrs4996815
1000 genomesrs4996815
hgdprs4996815
ensemblrs4996815
geneviewrs4996815
scholarrs4996815
googlers4996815
pharmgkbrs4996815
gwascentralrs4996815
openSNPrs4996815
23andMers4996815
SNPshotrs4996815
SNPdbers4996815
MSV3drs4996815
GWAS Ctlgrs4996815
GMAF0.4807
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 20889312]
Trait
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder
Risk Allele C
P-val 1E-7
Odds Ratio 1.28 [NR]