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rs150829393

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150829393(A;A)
Make rs150829393(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position84799209
GeneZNF592
is asnp
is mentioned by
dbSNPrs150829393
ebirs150829393
HLIrs150829393
Exacrs150829393
Varsomers150829393
Maprs150829393
PheGenIrs150829393
hapmaprs150829393
1000 genomesrs150829393
hgdprs150829393
ensemblrs150829393
gopubmedrs150829393
geneviewrs150829393
scholarrs150829393
googlers150829393
pharmgkbrs150829393
gwascentralrs150829393
openSNPrs150829393
23andMers150829393
23andMe allrs150829393
SNP Nexus

SNPshotrs150829393
SNPdbers150829393
MSV3drs150829393
GWAS Ctlgrs150829393
Max Magnitude0
ClinVar
Risk rs150829393(A;A)
Alt rs150829393(A;A)
Reference rs150829393(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia autosomal recessive 5
Variation info
Gene ZNF592
CLNDBN Spinocerebellar ataxia autosomal recessive 5
Reversed 0
HGVS NC_000015.9:g.85342440G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000014.3,