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rs864622269

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622269(C;T)
Make rs864622269(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position50628394
GeneATL1
is asnp
is mentioned by
dbSNPrs864622269
ebirs864622269
HLIrs864622269
Exacrs864622269
Varsomers864622269
Maprs864622269
PheGenIrs864622269
hapmaprs864622269
1000 genomesrs864622269
hgdprs864622269
ensemblrs864622269
gopubmedrs864622269
geneviewrs864622269
scholarrs864622269
googlers864622269
pharmgkbrs864622269
gwascentralrs864622269
openSNPrs864622269
23andMers864622269
23andMe allrs864622269
SNP Nexus

SNPshotrs864622269
SNPdbers864622269
MSV3drs864622269
GWAS Ctlgrs864622269
Max Magnitude0
ClinVar
Risk rs864622269(T;T)
Alt rs864622269(T;T)
Reference rs864622269(C;C)
Significance Pathogenic
Disease Spastic paraplegia 3
Variation info
Gene ATL1
CLNDBN Spastic paraplegia 3
Reversed 0
HGVS NC_000014.8:g.51095112C>T
CLNSRC
CLNACC RCV000203724.2,