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rs587776922

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776922(A;T)
Make rs587776922(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position26598397
GeneANO3
is asnp
is mentioned by
dbSNPrs587776922
ebirs587776922
HLIrs587776922
Exacrs587776922
Varsomers587776922
Maprs587776922
PheGenIrs587776922
hapmaprs587776922
1000 genomesrs587776922
hgdprs587776922
ensemblrs587776922
gopubmedrs587776922
geneviewrs587776922
scholarrs587776922
googlers587776922
pharmgkbrs587776922
gwascentralrs587776922
openSNPrs587776922
23andMers587776922
23andMe allrs587776922
SNP Nexus

SNPshotrs587776922
SNPdbers587776922
MSV3drs587776922
GWAS Ctlgrs587776922
Max Magnitude0
ClinVar
Risk rs587776922(T;T)
Alt rs587776922(T;T)
Reference rs587776922(A;A)
Significance Pathogenic
Disease Dystonia 24
Variation info
Gene ANO3
CLNDBN Dystonia 24
Reversed 0
HGVS NC_000011.9:g.26619944A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032692.2,