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rs3737597

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3737597(C;T)
Make rs3737597(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position232037092
GeneDISC1, MAP1LC3C
is asnp
is mentioned by
dbSNPrs3737597
ebirs3737597
HLIrs3737597
Exacrs3737597
Varsomers3737597
Maprs3737597
PheGenIrs3737597
hapmaprs3737597
1000 genomesrs3737597
hgdprs3737597
ensemblrs3737597
gopubmedrs3737597
geneviewrs3737597
scholarrs3737597
googlers3737597
pharmgkbrs3737597
gwascentralrs3737597
openSNPrs3737597
23andMers3737597
23andMe allrs3737597
SNP Nexus

SNPshotrs3737597
SNPdbers3737597
MSV3drs3737597
GWAS Ctlgrs3737597
GMAF0.07484
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 18818052] schizophrenia minor allele of rs3737597 (frequency 2%)

[PMID 19911060OA-icon.png] Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.