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rs587777670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777670(A;A)
Make rs587777670(A;C)
ReferenceGRCh38 38.1/142
Chromosome6
Position53270660
GeneELOVL5
is asnp
is mentioned by
dbSNPrs587777670
ebirs587777670
HLIrs587777670
Exacrs587777670
Varsomers587777670
Maprs587777670
PheGenIrs587777670
hapmaprs587777670
1000 genomesrs587777670
hgdprs587777670
ensemblrs587777670
gopubmedrs587777670
geneviewrs587777670
scholarrs587777670
googlers587777670
pharmgkbrs587777670
gwascentralrs587777670
openSNPrs587777670
23andMers587777670
23andMe allrs587777670
SNP Nexus

SNPshotrs587777670
SNPdbers587777670
MSV3drs587777670
GWAS Ctlgrs587777670
Max Magnitude0
ClinVar
Risk rs587777670(A,T;A,T)
Alt rs587777670(A,T;A,T)
Reference rs587777670(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia 38
Variation info
Gene ELOVL5
CLNDBN Spinocerebellar ataxia 38
Reversed 0
HGVS NC_000006.11:g.53135458C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000133587.2,