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rs137852524

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852524(A;A)
Make rs137852524(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position153869818
GeneL1CAM
is asnp
is mentioned by
dbSNPrs137852524
ebirs137852524
HLIrs137852524
Exacrs137852524
Varsomers137852524
Maprs137852524
PheGenIrs137852524
hapmaprs137852524
1000 genomesrs137852524
hgdprs137852524
ensemblrs137852524
gopubmedrs137852524
geneviewrs137852524
scholarrs137852524
googlers137852524
pharmgkbrs137852524
gwascentralrs137852524
openSNPrs137852524
23andMers137852524
23andMe allrs137852524
SNP Nexus

SNPshotrs137852524
SNPdbers137852524
MSV3drs137852524
GWAS Ctlgrs137852524
Max Magnitude0
OMIM308840
Desc
Variant0011
Relatedalso
ClinVar
Risk rs137852524(A;A)
Alt rs137852524(A;A)
Reference rs137852524(G;G)
Significance Pathogenic
Disease Spastic paraplegia 1
Variation info
Gene L1CAM
CLNDBN Spastic paraplegia 1
Reversed 1
HGVS NC_000023.10:g.153135273C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010677.4,