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rs863224494

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224494(A;T)
Make rs863224494(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153867800
GeneL1CAM
is asnp
is mentioned by
dbSNPrs863224494
ebirs863224494
HLIrs863224494
Exacrs863224494
Varsomers863224494
Maprs863224494
PheGenIrs863224494
hapmaprs863224494
1000 genomesrs863224494
hgdprs863224494
ensemblrs863224494
gopubmedrs863224494
geneviewrs863224494
scholarrs863224494
googlers863224494
pharmgkbrs863224494
gwascentralrs863224494
openSNPrs863224494
23andMers863224494
23andMe allrs863224494
SNP Nexus

SNPshotrs863224494
SNPdbers863224494
MSV3drs863224494
GWAS Ctlgrs863224494
Max Magnitude0
ClinVar
Risk rs863224494(T;T)
Alt rs863224494(T;T)
Reference rs863224494(A;A)
Significance Pathogenic
Disease Spastic paraplegia
Variation info
Gene L1CAM
CLNDBN Spastic paraplegia
Reversed 1
HGVS NC_000023.10:g.153133255T>A
CLNSRC
CLNACC RCV000195759.1,