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rs878853147

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853147(C;T)
Make rs878853147(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71169399
GeneNLGN3
is asnp
is mentioned by
dbSNPrs878853147
ebirs878853147
HLIrs878853147
Exacrs878853147
Varsomers878853147
Maprs878853147
PheGenIrs878853147
hapmaprs878853147
1000 genomesrs878853147
hgdprs878853147
ensemblrs878853147
gopubmedrs878853147
geneviewrs878853147
scholarrs878853147
googlers878853147
pharmgkbrs878853147
gwascentralrs878853147
openSNPrs878853147
23andMers878853147
23andMe allrs878853147
SNP Nexus

SNPshotrs878853147
SNPdbers878853147
MSV3drs878853147
GWAS Ctlgrs878853147
Max Magnitude0
ClinVar
Risk rs878853147(T;T)
Alt rs878853147(T;T)
Reference rs878853147(C;C)
Significance Probable-Pathogenic
Disease Intellectual disability
Variation info
Gene NLGN3
CLNDBN Intellectual disability
Reversed 0
HGVS NC_000023.10:g.70389249C>T
CLNSRC
CLNACC RCV000224769.1,