rs3747333

Orientation

minus

Stabilized

minus

Make rs3747333(C;C)

Make rs3747333(C;T)

Make rs3747333(T;T)

Reference

GRCh38 38.1/142

Chromosome

X

Position

5893491

Gene

NLGN4X

is a	snp
is	mentioned by
dbSNP	rs3747333
dbSNP (classic)	rs3747333
ClinGen	rs3747333
ebi	rs3747333
HLI	rs3747333
Exac	rs3747333
Gnomad	rs3747333
Varsome	rs3747333
LitVar	rs3747333
Map	rs3747333
PheGenI	rs3747333
Biobank	rs3747333
1000 genomes	rs3747333
hgdp	rs3747333
ensembl	rs3747333
geneview	rs3747333
scholar	rs3747333
google	rs3747333
pharmgkb	rs3747333
gwascentral	rs3747333
openSNP	rs3747333
23andMe	rs3747333
SNPshot	rs3747333
SNPdbe	rs3747333
MSV3d	rs3747333
GWAS Ctlg	rs3747333

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

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

ClinVar
Risk	rs3747333(G;G) rs3747333(T;T)
Alt	rs3747333(G;G) rs3747333(T;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,

[PMID 31139237] Analysis of the SNP rs3747333 and rs3747334 in NLGN4X gene in autism spectrum disorder: a meta-analysis.