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rs748809996

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748809996(C;T)
Make rs748809996(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position73602452
GenePDZRN3
is asnp
is mentioned by
dbSNPrs748809996
ebirs748809996
HLIrs748809996
Exacrs748809996
Varsomers748809996
Maprs748809996
PheGenIrs748809996
hapmaprs748809996
1000 genomesrs748809996
hgdprs748809996
ensemblrs748809996
gopubmedrs748809996
geneviewrs748809996
scholarrs748809996
googlers748809996
pharmgkbrs748809996
gwascentralrs748809996
openSNPrs748809996
23andMers748809996
23andMe allrs748809996
SNP Nexus

SNPshotrs748809996
SNPdbers748809996
MSV3drs748809996
GWAS Ctlgrs748809996
Max Magnitude0
ClinVar
Risk rs748809996(T;T)
Alt rs748809996(T;T)
Reference rs748809996(C;C)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene PDZRN3
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000003.11:g.73651603C>T
CLNSRC
CLNACC RCV000202335.1,