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rs869025292

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025292(C;T)
Make rs869025292(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position136412502
GenePMPCA, SDCCAG3
is asnp
is mentioned by
dbSNPrs869025292
ebirs869025292
HLIrs869025292
Exacrs869025292
Varsomers869025292
Maprs869025292
PheGenIrs869025292
hapmaprs869025292
1000 genomesrs869025292
hgdprs869025292
ensemblrs869025292
gopubmedrs869025292
geneviewrs869025292
scholarrs869025292
googlers869025292
pharmgkbrs869025292
gwascentralrs869025292
openSNPrs869025292
23andMers869025292
23andMe allrs869025292
SNP Nexus

SNPshotrs869025292
SNPdbers869025292
MSV3drs869025292
GWAS Ctlgrs869025292
Max Magnitude0
ClinVar
Risk rs869025292(T;T)
Alt rs869025292(T;T)
Reference rs869025292(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene PMPCA SDCCAG3
CLNDBN Spinocerebellar ataxia, autosomal recessive 2
Reversed 0
HGVS NC_000009.11:g.139306954C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000207255.1,