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rs398123362

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123362(-;-)
Make rs398123362(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153875814
GeneL1CAM
is asnp
is mentioned by
dbSNPrs398123362
ebirs398123362
HLIrs398123362
Exacrs398123362
Varsomers398123362
Maprs398123362
PheGenIrs398123362
hapmaprs398123362
1000 genomesrs398123362
hgdprs398123362
ensemblrs398123362
gopubmedrs398123362
geneviewrs398123362
scholarrs398123362
googlers398123362
pharmgkbrs398123362
gwascentralrs398123362
openSNPrs398123362
23andMers398123362
23andMe allrs398123362
SNP Nexus

SNPshotrs398123362
SNPdbers398123362
MSV3drs398123362
GWAS Ctlgrs398123362
Max Magnitude0
ClinVar
Risk rs398123362(;)
Alt rs398123362(;)
Reference rs398123362(T;T)
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.153141269delA
CLNSRC ClinVar
CLNACC RCV000078734.3, RCV000173129.1,