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rs3747333

From SNPedia

Orientationminus
Stabilizedminus
Make rs3747333(C;C)
Make rs3747333(C;T)
Make rs3747333(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position5893491
GeneNLGN4X
is asnp
is mentioned by
dbSNPrs3747333
ebirs3747333
HLIrs3747333
Exacrs3747333
Varsomers3747333
Maprs3747333
PheGenIrs3747333
hapmaprs3747333
1000 genomesrs3747333
hgdprs3747333
ensemblrs3747333
gopubmedrs3747333
geneviewrs3747333
scholarrs3747333
googlers3747333
pharmgkbrs3747333
gwascentralrs3747333
openSNPrs3747333
23andMers3747333
23andMe allrs3747333
SNP Nexus

SNPshotrs3747333
SNPdbers3747333
MSV3drs3747333
GWAS Ctlgrs3747333
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24570023] Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients

ClinVar
Risk rs3747333(G,T;G,T)
Alt rs3747333(G,T;G,T)
Reference rs3747333(C;C)
Significance Other
Disease not specified
Variation info
Gene NLGN4X
CLNDBN not specified
Reversed 1
HGVS NC_000023.10:g.5811532G>A
CLNSRC
CLNACC RCV000082034.7,