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rs398122928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122928(C;T)
Make rs398122928(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position11752494
GeneGNAL
is asnp
is mentioned by
dbSNPrs398122928
ebirs398122928
HLIrs398122928
Exacrs398122928
Varsomers398122928
Maprs398122928
PheGenIrs398122928
hapmaprs398122928
1000 genomesrs398122928
hgdprs398122928
ensemblrs398122928
gopubmedrs398122928
geneviewrs398122928
scholarrs398122928
googlers398122928
pharmgkbrs398122928
gwascentralrs398122928
openSNPrs398122928
23andMers398122928
23andMe allrs398122928
SNP Nexus

SNPshotrs398122928
SNPdbers398122928
MSV3drs398122928
GWAS Ctlgrs398122928
Max Magnitude0
ClinVar
Risk rs398122928(T;T)
Alt rs398122928(T;T)
Reference rs398122928(C;C)
Significance Pathogenic
Disease Dystonia 25
Variation info
Gene GNAL
CLNDBN Dystonia 25
Reversed 0
HGVS NC_000018.9:g.11752493C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033106.26,