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rs863224927

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224927(G;T)
Make rs863224927(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position152433794
GeneSYNE1
is asnp
is mentioned by
dbSNPrs863224927
ebirs863224927
HLIrs863224927
Exacrs863224927
Varsomers863224927
Maprs863224927
PheGenIrs863224927
hapmaprs863224927
1000 genomesrs863224927
hgdprs863224927
ensemblrs863224927
gopubmedrs863224927
geneviewrs863224927
scholarrs863224927
googlers863224927
pharmgkbrs863224927
gwascentralrs863224927
openSNPrs863224927
23andMers863224927
23andMe allrs863224927
SNP Nexus

SNPshotrs863224927
SNPdbers863224927
MSV3drs863224927
GWAS Ctlgrs863224927
Max Magnitude0
ClinVar
Risk rs863224927(T;T)
Alt rs863224927(T;T)
Reference rs863224927(G;G)
Significance Probable-Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SYNE1
CLNDBN Spinocerebellar ataxia, autosomal recessive 8
Reversed 1
HGVS NC_000006.11:g.152754929C>A
CLNSRC
CLNACC RCV000197641.1,