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rs397514712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514712(A;A)
Make rs397514712(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position50628155
GeneATL1
is asnp
is mentioned by
dbSNPrs397514712
ebirs397514712
HLIrs397514712
Exacrs397514712
Varsomers397514712
Maprs397514712
PheGenIrs397514712
hapmaprs397514712
1000 genomesrs397514712
hgdprs397514712
ensemblrs397514712
gopubmedrs397514712
geneviewrs397514712
scholarrs397514712
googlers397514712
pharmgkbrs397514712
gwascentralrs397514712
openSNPrs397514712
23andMers397514712
23andMe allrs397514712
SNP Nexus

SNPshotrs397514712
SNPdbers397514712
MSV3drs397514712
GWAS Ctlgrs397514712
Max Magnitude0
ClinVar
Risk rs397514712(A;A)
Alt rs397514712(A;A)
Reference rs397514712(G;G)
Significance Pathogenic
Disease Spastic paraplegia 3
Variation info
Gene ATL1
CLNDBN Spastic paraplegia 3
Reversed 0
HGVS NC_000014.8:g.51094873G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000050231.3,