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rs387906933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906933(C;T)
Make rs387906933(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position50698797
GeneSHANK3
is asnp
is mentioned by
dbSNPrs387906933
ebirs387906933
HLIrs387906933
Exacrs387906933
Varsomers387906933
Maprs387906933
PheGenIrs387906933
hapmaprs387906933
1000 genomesrs387906933
hgdprs387906933
ensemblrs387906933
gopubmedrs387906933
geneviewrs387906933
scholarrs387906933
googlers387906933
pharmgkbrs387906933
gwascentralrs387906933
openSNPrs387906933
23andMers387906933
23andMe allrs387906933
SNP Nexus

SNPshotrs387906933
SNPdbers387906933
MSV3drs387906933
GWAS Ctlgrs387906933
Max Magnitude0
ClinVar
Risk rs387906933(T;T)
Alt rs387906933(T;T)
Reference rs387906933(C;C)
Significance Pathogenic
Disease Schizophrenia 15
Variation info
Gene SHANK3
CLNDBN Schizophrenia 15
Reversed 0
HGVS NC_000022.10:g.51137225C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023520.2,