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rs587777345

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777345(C;C)
Make rs587777345(C;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position682214
GeneJMJD8, STUB1
is asnp
is mentioned by
dbSNPrs587777345
ebirs587777345
HLIrs587777345
Exacrs587777345
Varsomers587777345
Maprs587777345
PheGenIrs587777345
hapmaprs587777345
1000 genomesrs587777345
hgdprs587777345
ensemblrs587777345
gopubmedrs587777345
geneviewrs587777345
scholarrs587777345
googlers587777345
pharmgkbrs587777345
gwascentralrs587777345
openSNPrs587777345
23andMers587777345
23andMe allrs587777345
SNP Nexus

SNPshotrs587777345
SNPdbers587777345
MSV3drs587777345
GWAS Ctlgrs587777345
Max Magnitude0
ClinVar
Risk rs587777345(C;C)
Alt rs587777345(C;C)
Reference rs587777345(T;T)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene JMJD8 STUB1
CLNDBN Spinocerebellar ataxia, autosomal recessive 16
Reversed 0
HGVS NC_000016.9:g.732214T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000115003.3,