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rs587777346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777346(A;A)
Make rs587777346(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position681227
GeneJMJD8, STUB1
is asnp
is mentioned by
dbSNPrs587777346
ebirs587777346
HLIrs587777346
Exacrs587777346
Varsomers587777346
Maprs587777346
PheGenIrs587777346
hapmaprs587777346
1000 genomesrs587777346
hgdprs587777346
ensemblrs587777346
gopubmedrs587777346
geneviewrs587777346
scholarrs587777346
googlers587777346
pharmgkbrs587777346
gwascentralrs587777346
openSNPrs587777346
23andMers587777346
23andMe allrs587777346
SNP Nexus

SNPshotrs587777346
SNPdbers587777346
MSV3drs587777346
GWAS Ctlgrs587777346
Max Magnitude0
ClinVar
Risk rs587777346(A;A)
Alt rs587777346(A;A)
Reference rs587777346(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene JMJD8 STUB1 LOC105371184
CLNDBN Spinocerebellar ataxia, autosomal recessive 16
Reversed 0
HGVS NC_000016.9:g.731227G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000115004.3,