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rs587776923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776923(A;G)
Make rs587776923(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position26639153
GeneANO3
is asnp
is mentioned by
dbSNPrs587776923
ebirs587776923
HLIrs587776923
Exacrs587776923
Varsomers587776923
Maprs587776923
PheGenIrs587776923
hapmaprs587776923
1000 genomesrs587776923
hgdprs587776923
ensemblrs587776923
gopubmedrs587776923
geneviewrs587776923
scholarrs587776923
googlers587776923
pharmgkbrs587776923
gwascentralrs587776923
openSNPrs587776923
23andMers587776923
23andMe allrs587776923
SNP Nexus

SNPshotrs587776923
SNPdbers587776923
MSV3drs587776923
GWAS Ctlgrs587776923
Max Magnitude0
ClinVar
Risk rs587776923(G;G)
Alt rs587776923(G;G)
Reference rs587776923(A;A)
Significance Pathogenic
Disease Dystonia 24
Variation info
Gene ANO3
CLNDBN Dystonia 24
Reversed 0
HGVS NC_000011.9:g.26660700A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000032694.2,