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rs878853158

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853158(G;T)
Make rs878853158(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position77211229
GenePDE8B
is asnp
is mentioned by
dbSNPrs878853158
ebirs878853158
HLIrs878853158
Exacrs878853158
Varsomers878853158
Maprs878853158
PheGenIrs878853158
hapmaprs878853158
1000 genomesrs878853158
hgdprs878853158
ensemblrs878853158
gopubmedrs878853158
geneviewrs878853158
scholarrs878853158
googlers878853158
pharmgkbrs878853158
gwascentralrs878853158
openSNPrs878853158
23andMers878853158
23andMe allrs878853158
SNP Nexus

SNPshotrs878853158
SNPdbers878853158
MSV3drs878853158
GWAS Ctlgrs878853158
Max Magnitude0
ClinVar
Risk rs878853158(T;T)
Alt rs878853158(T;T)
Reference rs878853158(G;G)
Significance Pathogenic
Disease Striatal degeneration
Variation info
Gene PDE8B
CLNDBN Striatal degeneration, autosomal dominant
Reversed 0
HGVS NC_000005.9:g.76507054G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000224977.1,