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rs398122925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122925(A;A)
Make rs398122925(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position11824987
GeneGNAL
is asnp
is mentioned by
dbSNPrs398122925
ebirs398122925
HLIrs398122925
Exacrs398122925
Varsomers398122925
Maprs398122925
PheGenIrs398122925
hapmaprs398122925
1000 genomesrs398122925
hgdprs398122925
ensemblrs398122925
gopubmedrs398122925
geneviewrs398122925
scholarrs398122925
googlers398122925
pharmgkbrs398122925
gwascentralrs398122925
openSNPrs398122925
23andMers398122925
23andMe allrs398122925
SNP Nexus

SNPshotrs398122925
SNPdbers398122925
MSV3drs398122925
GWAS Ctlgrs398122925
Max Magnitude0
ClinVar
Risk rs398122925(A;A)
Alt rs398122925(A;A)
Reference rs398122925(G;G)
Significance Pathogenic
Disease Dystonia 25
Variation info
Gene GNAL
CLNDBN Dystonia 25
Reversed 0
HGVS NC_000018.9:g.11824986G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033103.26,