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rs863223353

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223353(C;T)
Make rs863223353(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position130499898
GeneMEST
is asnp
is mentioned by
dbSNPrs863223353
ebirs863223353
HLIrs863223353
Exacrs863223353
Varsomers863223353
Maprs863223353
PheGenIrs863223353
hapmaprs863223353
1000 genomesrs863223353
hgdprs863223353
ensemblrs863223353
gopubmedrs863223353
geneviewrs863223353
scholarrs863223353
googlers863223353
pharmgkbrs863223353
gwascentralrs863223353
openSNPrs863223353
23andMers863223353
23andMe allrs863223353
SNP Nexus

SNPshotrs863223353
SNPdbers863223353
MSV3drs863223353
GWAS Ctlgrs863223353
Max Magnitude0
ClinVar
Risk rs863223353(T;T)
Alt rs863223353(T;T)
Reference rs863223353(C;C)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene MEST
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000007.13:g.130139739C>T
CLNSRC
CLNACC RCV000202328.1,