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rs4778334

From SNPedia

Orientationplus
Stabilizedminus
Make rs4778334(A;A)
Make rs4778334(A;G)
Make rs4778334(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position22832212
is asnp
is mentioned by
dbSNPrs4778334
dbSNP (classic)rs4778334
ClinGenrs4778334
ebirs4778334
HLIrs4778334
Exacrs4778334
Gnomadrs4778334
Varsomers4778334
LitVarrs4778334
Maprs4778334
PheGenIrs4778334
Biobankrs4778334
1000 genomesrs4778334
hgdprs4778334
ensemblrs4778334
geneviewrs4778334
scholarrs4778334
googlers4778334
pharmgkbrs4778334
gwascentralrs4778334
openSNPrs4778334
23andMers4778334
23andMe allrs4778334
SNPshotrs4778334
SNPdbers4778334
MSV3drs4778334
GWAS Ctlgrs4778334
GMAF0.2291
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 22317777OA-icon.png] Rare CNVs and Tag SNPs at 15q11.2 Are Associated With Schizophrenia in the Han Chinese Population