rs398123364

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs398123364(-;-)

Make rs398123364(-;A)

Reference

GRCh38 38.1/141

Chromosome

X

Position

153864988

Gene

L1CAM

is a	snp
is	mentioned by
dbSNP	rs398123364
dbSNP (classic)	rs398123364
ClinGen	rs398123364
ebi	rs398123364
HLI	rs398123364
Exac	rs398123364
Gnomad	rs398123364
Varsome	rs398123364
LitVar	rs398123364
Map	rs398123364
PheGenI	rs398123364
Biobank	rs398123364
1000 genomes	rs398123364
hgdp	rs398123364
ensembl	rs398123364
geneview	rs398123364
scholar	rs398123364
google	rs398123364
pharmgkb	rs398123364
gwascentral	rs398123364
openSNP	rs398123364
23andMe	rs398123364
SNPshot	rs398123364
SNPdbe	rs398123364
MSV3d	rs398123364
GWAS Ctlg	rs398123364

Max Magnitude

0

ClinVar
Risk	rs398123364(-;-)
Alt	rs398123364(-;-)
Reference	Rs398123364(A;A)
Significance	Pathogenic
Disease	not provided X-linked hydrocephalus syndrome
Variation	info
Gene	L1CAM
CLNDBN	not provided X-linked hydrocephalus syndrome
Reversed	1
HGVS	NC_000023.10:g.153130443delT
CLNSRC	ClinVar
CLNACC	RCV000078737.3, RCV000176265.1,