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rs587777671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777671(C;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position53291808
GeneELOVL5
is asnp
is mentioned by
dbSNPrs587777671
ebirs587777671
HLIrs587777671
Exacrs587777671
Varsomers587777671
Maprs587777671
PheGenIrs587777671
hapmaprs587777671
1000 genomesrs587777671
hgdprs587777671
ensemblrs587777671
gopubmedrs587777671
geneviewrs587777671
scholarrs587777671
googlers587777671
pharmgkbrs587777671
gwascentralrs587777671
openSNPrs587777671
23andMers587777671
23andMe allrs587777671
SNP Nexus

SNPshotrs587777671
SNPdbers587777671
MSV3drs587777671
GWAS Ctlgrs587777671
Max Magnitude0
ClinVar
Risk rs587777671(G;G)
Alt rs587777671(G;G)
Reference rs587777671(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia 38
Variation info
Gene ELOVL5
CLNDBN Spinocerebellar ataxia 38
Reversed 1
HGVS NC_000006.11:g.53156606G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133588.2,