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

rs863224919

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224919(A;A)
Make rs863224919(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132295872
GeneSETX
is asnp
is mentioned by
dbSNPrs863224919
ebirs863224919
HLIrs863224919
Exacrs863224919
Varsomers863224919
Maprs863224919
PheGenIrs863224919
hapmaprs863224919
1000 genomesrs863224919
hgdprs863224919
ensemblrs863224919
gopubmedrs863224919
geneviewrs863224919
scholarrs863224919
googlers863224919
pharmgkbrs863224919
gwascentralrs863224919
openSNPrs863224919
23andMers863224919
23andMe allrs863224919
SNP Nexus

SNPshotrs863224919
SNPdbers863224919
MSV3drs863224919
GWAS Ctlgrs863224919
Max Magnitude0
ClinVar
Risk rs863224919(A;A)
Alt rs863224919(A;A)
Reference rs863224919(G;G)
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.135171259C>T
CLNSRC
CLNACC RCV000200211.1,