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rs398122924

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122924(A;A)
Make rs398122924(A;C)
ReferenceGRCh38 38.1/141
Chromosome18
Position11872345
GeneGNAL
is asnp
is mentioned by
dbSNPrs398122924
ebirs398122924
HLIrs398122924
Exacrs398122924
Varsomers398122924
Maprs398122924
PheGenIrs398122924
hapmaprs398122924
1000 genomesrs398122924
hgdprs398122924
ensemblrs398122924
gopubmedrs398122924
geneviewrs398122924
scholarrs398122924
googlers398122924
pharmgkbrs398122924
gwascentralrs398122924
openSNPrs398122924
23andMers398122924
23andMe allrs398122924
SNP Nexus

SNPshotrs398122924
SNPdbers398122924
MSV3drs398122924
GWAS Ctlgrs398122924
Max Magnitude0
ClinVar
Risk rs398122924(A;A)
Alt rs398122924(A;A)
Reference rs398122924(C;C)
Significance Pathogenic
Disease Dystonia 25
Variation info
Gene GNAL
CLNDBN Dystonia 25
Reversed 0
HGVS NC_000018.9:g.11872344C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033102.26,