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rs863223314

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223314(-;A)
Make rs863223314(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position50628430
GeneATL1
is asnp
is mentioned by
dbSNPrs863223314
dbSNP (old)rs863223314
ClinGenrs863223314
ebirs863223314
HLIrs863223314
Exacrs863223314
Gnomadrs863223314
Varsomers863223314
Maprs863223314
PheGenIrs863223314
Biobankrs863223314
1000 genomesrs863223314
hgdprs863223314
ensemblrs863223314
gopubmedrs863223314
geneviewrs863223314
scholarrs863223314
googlers863223314
pharmgkbrs863223314
gwascentralrs863223314
openSNPrs863223314
23andMers863223314
23andMe allrs863223314
SNP Nexus

SNPshotrs863223314
SNPdbers863223314
MSV3drs863223314
GWAS Ctlgrs863223314
Max Magnitude0
ClinVar
Risk rs863223314(A;A)
Alt rs863223314(A;A)
Reference Rs863223314(-;-)
Significance Pathogenic
Disease Spastic paraplegia 3
Variation info
Gene ATL1
CLNDBN Spastic paraplegia 3
Reversed 0
HGVS NC_000014.8:g.51095148dupA
CLNSRC
CLNACC RCV000020718.1,