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rs137852525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852525(A;A)
Make rs137852525(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153866826
GeneL1CAM
is asnp
is mentioned by
dbSNPrs137852525
ebirs137852525
HLIrs137852525
Exacrs137852525
Varsomers137852525
Maprs137852525
PheGenIrs137852525
hapmaprs137852525
1000 genomesrs137852525
hgdprs137852525
ensemblrs137852525
gopubmedrs137852525
geneviewrs137852525
scholarrs137852525
googlers137852525
pharmgkbrs137852525
gwascentralrs137852525
openSNPrs137852525
23andMers137852525
23andMe allrs137852525
SNP Nexus

SNPshotrs137852525
SNPdbers137852525
MSV3drs137852525
GWAS Ctlgrs137852525
Max Magnitude0
OMIM308840
Desc
Variant0014
Relatedalso
ClinVar
Risk rs137852525(A;A)
Alt rs137852525(A;A)
Reference rs137852525(G;G)
Significance Pathogenic
Disease Hydrocephalus
Variation info
Gene L1CAM
CLNDBN Hydrocephalus, X-linked, with hirschsprung disease
Reversed 1
HGVS NC_000023.10:g.153132281C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010680.4,