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rs863223346

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223346(A;A)
Make rs863223346(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position38876091
GeneFREM2
is asnp
is mentioned by
dbSNPrs863223346
ebirs863223346
HLIrs863223346
Exacrs863223346
Varsomers863223346
Maprs863223346
PheGenIrs863223346
hapmaprs863223346
1000 genomesrs863223346
hgdprs863223346
ensemblrs863223346
gopubmedrs863223346
geneviewrs863223346
scholarrs863223346
googlers863223346
pharmgkbrs863223346
gwascentralrs863223346
openSNPrs863223346
23andMers863223346
23andMe allrs863223346
SNP Nexus

SNPshotrs863223346
SNPdbers863223346
MSV3drs863223346
GWAS Ctlgrs863223346
Max Magnitude0
ClinVar
Risk rs863223346(A;A)
Alt rs863223346(A;A)
Reference rs863223346(G;G)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene FREM2
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000013.10:g.39450228G>A
CLNSRC
CLNACC RCV000202338.1,