Have questions? Visit https://www.reddit.com/r/SNPedia

rs781821239

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781821239(C;G)
Make rs781821239(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77040103
GeneB3GNT6
is asnp
is mentioned by
dbSNPrs781821239
ebirs781821239
HLIrs781821239
Exacrs781821239
Varsomers781821239
Maprs781821239
PheGenIrs781821239
hapmaprs781821239
1000 genomesrs781821239
hgdprs781821239
ensemblrs781821239
gopubmedrs781821239
geneviewrs781821239
scholarrs781821239
googlers781821239
pharmgkbrs781821239
gwascentralrs781821239
openSNPrs781821239
23andMers781821239
23andMe allrs781821239
SNP Nexus

SNPshotrs781821239
SNPdbers781821239
MSV3drs781821239
GWAS Ctlgrs781821239
Max Magnitude0
ClinVar
Risk rs781821239(G;G)
Alt rs781821239(G;G)
Reference rs781821239(C;C)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene B3GNT6
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000011.9:g.76751147C>G
CLNSRC
CLNACC RCV000202346.1,