Have questions? Visit https://www.reddit.com/r/SNPedia

rs864622083

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622083(A;A)
Make rs864622083(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position50628104
GeneATL1
is asnp
is mentioned by
dbSNPrs864622083
ebirs864622083
HLIrs864622083
Exacrs864622083
Varsomers864622083
Maprs864622083
PheGenIrs864622083
hapmaprs864622083
1000 genomesrs864622083
hgdprs864622083
ensemblrs864622083
gopubmedrs864622083
geneviewrs864622083
scholarrs864622083
googlers864622083
pharmgkbrs864622083
gwascentralrs864622083
openSNPrs864622083
23andMers864622083
23andMe allrs864622083
SNP Nexus

SNPshotrs864622083
SNPdbers864622083
MSV3drs864622083
GWAS Ctlgrs864622083
Max Magnitude0
ClinVar
Risk rs864622083(A;A)
Alt rs864622083(A;A)
Reference rs864622083(C;C)
Significance Probable-Pathogenic
Disease Spastic paraplegia 3
Variation info
Gene ATL1
CLNDBN Spastic paraplegia 3
Reversed 0
HGVS NC_000014.8:g.51094822C>A
CLNSRC
CLNACC RCV000203941.1,