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rs776061422

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776061422(A;A)
Make rs776061422(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position6254689
GeneGPR153
is asnp
is mentioned by
dbSNPrs776061422
ebirs776061422
HLIrs776061422
Exacrs776061422
Varsomers776061422
Maprs776061422
PheGenIrs776061422
hapmaprs776061422
1000 genomesrs776061422
hgdprs776061422
ensemblrs776061422
gopubmedrs776061422
geneviewrs776061422
scholarrs776061422
googlers776061422
pharmgkbrs776061422
gwascentralrs776061422
openSNPrs776061422
23andMers776061422
23andMe allrs776061422
SNP Nexus

SNPshotrs776061422
SNPdbers776061422
MSV3drs776061422
GWAS Ctlgrs776061422
Max Magnitude0
ClinVar
Risk rs776061422(A;A)
Alt rs776061422(A;A)
Reference rs776061422(G;G)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene GPR153
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000001.10:g.6314749G>A
CLNSRC
CLNACC RCV000202336.1,