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rs587777342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777342(G;T)
Make rs587777342(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position681520
GeneJMJD8, STUB1
is asnp
is mentioned by
dbSNPrs587777342
ebirs587777342
HLIrs587777342
Exacrs587777342
Varsomers587777342
Maprs587777342
PheGenIrs587777342
hapmaprs587777342
1000 genomesrs587777342
hgdprs587777342
ensemblrs587777342
gopubmedrs587777342
geneviewrs587777342
scholarrs587777342
googlers587777342
pharmgkbrs587777342
gwascentralrs587777342
openSNPrs587777342
23andMers587777342
23andMe allrs587777342
SNP Nexus

SNPshotrs587777342
SNPdbers587777342
MSV3drs587777342
GWAS Ctlgrs587777342
Max Magnitude0
ClinVar
Risk rs587777342(A,T;A,T)
Alt rs587777342(A,T;A,T)
Reference rs587777342(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.731520G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000115000.3,