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rs398122927

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122927(-;-)
Make rs398122927(-;A)
Make rs398122927(A;A)
ReferenceGRCh38 38.1/141
Chromosome18
Position11864577
GeneGNAL
is asnp
is mentioned by
dbSNPrs398122927
ebirs398122927
HLIrs398122927
Exacrs398122927
Varsomers398122927
Maprs398122927
PheGenIrs398122927
hapmaprs398122927
1000 genomesrs398122927
hgdprs398122927
ensemblrs398122927
gopubmedrs398122927
geneviewrs398122927
scholarrs398122927
googlers398122927
pharmgkbrs398122927
gwascentralrs398122927
openSNPrs398122927
23andMers398122927
23andMe allrs398122927
SNP Nexus

SNPshotrs398122927
SNPdbers398122927
MSV3drs398122927
GWAS Ctlgrs398122927
Max Magnitude0
ClinVar
Risk rs398122927(A;A)
Alt rs398122927(A;A)
Reference rs398122927(;)
Significance Pathogenic
Disease Dystonia 25
Variation info
Gene GNAL
CLNDBN Dystonia 25
Reversed 0
HGVS NC_000018.9:g.11864576dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000033105.24,