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rs397509359

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509359(C;T)
Make rs397509359(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position71529785
GeneTAF1
is asnp
is mentioned by
dbSNPrs397509359
ebirs397509359
HLIrs397509359
Exacrs397509359
Varsomers397509359
Maprs397509359
PheGenIrs397509359
hapmaprs397509359
1000 genomesrs397509359
hgdprs397509359
ensemblrs397509359
gopubmedrs397509359
geneviewrs397509359
scholarrs397509359
googlers397509359
pharmgkbrs397509359
gwascentralrs397509359
openSNPrs397509359
23andMers397509359
23andMe allrs397509359
SNP Nexus

SNPshotrs397509359
SNPdbers397509359
MSV3drs397509359
GWAS Ctlgrs397509359
Max Magnitude0
ClinVar
Risk rs397509359(T;T)
Alt rs397509359(T;T)
Reference rs397509359(C;C)
Significance Pathogenic
Disease Dystonia 3
Variation info
Gene TAF1
CLNDBN Dystonia 3, torsion, X-linked
Reversed 0
HGVS NC_000023.10:g.70749635C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020067.1,