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rs387906932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906932(C;T)
Make rs387906932(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position50721182
GeneSHANK3
is asnp
is mentioned by
dbSNPrs387906932
ebirs387906932
HLIrs387906932
Exacrs387906932
Varsomers387906932
Maprs387906932
PheGenIrs387906932
hapmaprs387906932
1000 genomesrs387906932
hgdprs387906932
ensemblrs387906932
gopubmedrs387906932
geneviewrs387906932
scholarrs387906932
googlers387906932
pharmgkbrs387906932
gwascentralrs387906932
openSNPrs387906932
23andMers387906932
23andMe allrs387906932
SNP Nexus

SNPshotrs387906932
SNPdbers387906932
MSV3drs387906932
GWAS Ctlgrs387906932
Max Magnitude0
ClinVar
Risk rs387906932(T;T)
Alt rs387906932(T;T)
Reference rs387906932(C;C)
Significance Pathogenic
Disease Schizophrenia 15
Variation info
Gene SHANK3
CLNDBN Schizophrenia 15
Reversed 0
HGVS NC_000022.10:g.51159610C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023519.3,