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rs863223352

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223352(G;T)
Make rs863223352(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position81683794
GeneARL16, HGS
is asnp
is mentioned by
dbSNPrs863223352
ebirs863223352
HLIrs863223352
Exacrs863223352
Varsomers863223352
Maprs863223352
PheGenIrs863223352
hapmaprs863223352
1000 genomesrs863223352
hgdprs863223352
ensemblrs863223352
gopubmedrs863223352
geneviewrs863223352
scholarrs863223352
googlers863223352
pharmgkbrs863223352
gwascentralrs863223352
openSNPrs863223352
23andMers863223352
23andMe allrs863223352
SNP Nexus

SNPshotrs863223352
SNPdbers863223352
MSV3drs863223352
GWAS Ctlgrs863223352
Max Magnitude0
ClinVar
Risk rs863223352(T;T)
Alt rs863223352(T;T)
Reference rs863223352(G;G)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene HGS ARL16
CLNDBN Childhood-Onset Schizophrenia
Reversed 1
HGVS NC_000017.10:g.79650824C>A
CLNSRC
CLNACC RCV000202347.1,