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

rs4500567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4500567(C;C)
Make rs4500567(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position71166082
is asnp
is mentioned by
dbSNPrs4500567
ebirs4500567
HLIrs4500567
Exacrs4500567
Varsomers4500567
Maprs4500567
PheGenIrs4500567
hapmaprs4500567
1000 genomesrs4500567
hgdprs4500567
ensemblrs4500567
gopubmedrs4500567
geneviewrs4500567
scholarrs4500567
googlers4500567
pharmgkbrs4500567
gwascentralrs4500567
openSNPrs4500567
23andMers4500567
23andMe allrs4500567
SNP Nexus

SNPshotrs4500567
SNPdbers4500567
MSV3drs4500567
GWAS Ctlgrs4500567
GMAF0.1359
Max Magnitude0
? (C;C) (C;G) (G;G) 28

[PMID 20052686] Functional variants of TSPAN8 are associated with bipolar disorder and schizophrenia