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

rs797045068

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045068(G;G)
Make rs797045068(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132295940
GeneSETX
is asnp
is mentioned by
dbSNPrs797045068
ebirs797045068
HLIrs797045068
Exacrs797045068
Varsomers797045068
Maprs797045068
PheGenIrs797045068
hapmaprs797045068
1000 genomesrs797045068
hgdprs797045068
ensemblrs797045068
gopubmedrs797045068
geneviewrs797045068
scholarrs797045068
googlers797045068
pharmgkbrs797045068
gwascentralrs797045068
openSNPrs797045068
23andMers797045068
23andMe allrs797045068
SNP Nexus

SNPshotrs797045068
SNPdbers797045068
MSV3drs797045068
GWAS Ctlgrs797045068
Max Magnitude0
ClinVar
Risk rs797045068(G;G)
Alt rs797045068(G;G)
Reference rs797045068(T;T)
Significance Probable-Pathogenic
Disease Spinocerebellar ataxia autosomal recessive 1
Variation info
Gene SETX
CLNDBN Spinocerebellar ataxia autosomal recessive 1
Reversed 1
HGVS NC_000009.11:g.135171327A>C
CLNSRC Baylor College of Medicine
CLNACC RCV000191127.2,