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rs433598

From SNPedia

Orientationplus
Stabilizedplus
Make rs433598(C;C)
Make rs433598(C;T)
Make rs433598(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position20668884
GeneACSM1
is asnp
is mentioned by
dbSNPrs433598
ebirs433598
HLIrs433598
Exacrs433598
Varsomers433598
Maprs433598
PheGenIrs433598
hapmaprs433598
1000 genomesrs433598
hgdprs433598
ensemblrs433598
gopubmedrs433598
geneviewrs433598
scholarrs433598
googlers433598
pharmgkbrs433598
gwascentralrs433598
openSNPrs433598
23andMers433598
23andMe allrs433598
SNP Nexus

SNPshotrs433598
SNPdbers433598
MSV3drs433598
GWAS Ctlgrs433598
GMAF0.4096
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20185149OA-icon.png]
Trait Schizophrenia
Title Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.
Risk Allele T
P-val 0.000003
Odds Ratio 1.13 [NR]


[PMID 25656805] Genetic association of ACSM1 variation with schizophrenia and major depressive disorder in the Han Chinese population