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rs137852657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852657(C;T)
Make rs137852657(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position50591584
GeneATL1
is asnp
is mentioned by
dbSNPrs137852657
ebirs137852657
HLIrs137852657
Exacrs137852657
Varsomers137852657
Maprs137852657
PheGenIrs137852657
hapmaprs137852657
1000 genomesrs137852657
hgdprs137852657
ensemblrs137852657
gopubmedrs137852657
geneviewrs137852657
scholarrs137852657
googlers137852657
pharmgkbrs137852657
gwascentralrs137852657
openSNPrs137852657
23andMers137852657
23andMe allrs137852657
SNP Nexus

SNPshotrs137852657
SNPdbers137852657
MSV3drs137852657
GWAS Ctlgrs137852657
Max Magnitude0
ClinVar
Risk rs137852657(T;T)
Alt rs137852657(T;T)
Reference rs137852657(C;C)
Significance Pathogenic
Disease Spastic paraplegia 3
Variation info
Gene ATL1
CLNDBN Spastic paraplegia 3
Reversed 0
HGVS NC_000014.8:g.51058302C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020721.2,