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rs398122926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122926(-;-)
Make rs398122926(-;T)
Make rs398122926(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position11753835
GeneGNAL
is asnp
is mentioned by
dbSNPrs398122926
ebirs398122926
HLIrs398122926
Exacrs398122926
Varsomers398122926
Maprs398122926
PheGenIrs398122926
hapmaprs398122926
1000 genomesrs398122926
hgdprs398122926
ensemblrs398122926
gopubmedrs398122926
geneviewrs398122926
scholarrs398122926
googlers398122926
pharmgkbrs398122926
gwascentralrs398122926
openSNPrs398122926
23andMers398122926
23andMe allrs398122926
SNP Nexus

SNPshotrs398122926
SNPdbers398122926
MSV3drs398122926
GWAS Ctlgrs398122926
Max Magnitude0
ClinVar
Risk rs398122926(T;T)
Alt rs398122926(T;T)
Reference rs398122926(;)
Significance Pathogenic
Disease Dystonia 25
Variation info
Gene GNAL
CLNDBN Dystonia 25
Reversed 0
HGVS NC_000018.9:g.11753834dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000033104.24,