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rs3747334

From SNPedia

Orientationminus
Stabilizedminus
Make rs3747334(C;C)
Make rs3747334(C;G)
Make rs3747334(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position5893489
GeneNLGN4X
is asnp
is mentioned by
dbSNPrs3747334
ebirs3747334
HLIrs3747334
Exacrs3747334
Varsomers3747334
Maprs3747334
PheGenIrs3747334
hapmaprs3747334
1000 genomesrs3747334
hgdprs3747334
ensemblrs3747334
gopubmedrs3747334
geneviewrs3747334
scholarrs3747334
googlers3747334
pharmgkbrs3747334
gwascentralrs3747334
openSNPrs3747334
23andMers3747334
23andMe allrs3747334
SNP Nexus

SNPshotrs3747334
SNPdbers3747334
MSV3drs3747334
GWAS Ctlgrs3747334
Max Magnitude

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

ClinVar
Risk rs3747334(A,G,T;A,G,T)
Alt rs3747334(A,G,T;A,G,T)
Reference rs3747334(C;C)
Significance Other
Disease not specified
Variation info
Gene NLGN4X
CLNDBN not specified
Reversed 1
HGVS NC_000023.10:g.5811530G>C
CLNSRC
CLNACC RCV000082035.7,