Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606665(C;C)
Make rs267606665(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position32984733
GeneAPTX
is asnp
is mentioned by
dbSNPrs267606665
ebirs267606665
HLIrs267606665
Exacrs267606665
Varsomers267606665
Maprs267606665
PheGenIrs267606665
hapmaprs267606665
1000 genomesrs267606665
hgdprs267606665
ensemblrs267606665
gopubmedrs267606665
geneviewrs267606665
scholarrs267606665
googlers267606665
pharmgkbrs267606665
gwascentralrs267606665
openSNPrs267606665
23andMers267606665
23andMe allrs267606665
SNP Nexus

SNPshotrs267606665
SNPdbers267606665
MSV3drs267606665
GWAS Ctlgrs267606665
Max Magnitude0
ClinVar
Risk rs267606665(C;C)
Alt rs267606665(C;C)
Reference rs267606665(T;T)
Significance Pathogenic
Disease Adult onset ataxia with oculomotor apraxia
Variation info
Gene APTX
CLNDBN Adult onset ataxia with oculomotor apraxia
Reversed 1
HGVS NC_000009.11:g.32984731A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004683.2,