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rs398123364

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123364(-;-)
Make rs398123364(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153864988
GeneL1CAM
is asnp
is mentioned by
dbSNPrs398123364
ebirs398123364
HLIrs398123364
Exacrs398123364
Varsomers398123364
Maprs398123364
PheGenIrs398123364
hapmaprs398123364
1000 genomesrs398123364
hgdprs398123364
ensemblrs398123364
gopubmedrs398123364
geneviewrs398123364
scholarrs398123364
googlers398123364
pharmgkbrs398123364
gwascentralrs398123364
openSNPrs398123364
23andMers398123364
23andMe allrs398123364
SNP Nexus

SNPshotrs398123364
SNPdbers398123364
MSV3drs398123364
GWAS Ctlgrs398123364
Max Magnitude0
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,