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rs863224928

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224928(A;A)
Make rs863224928(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position152391364
GeneSYNE1
is asnp
is mentioned by
dbSNPrs863224928
ebirs863224928
HLIrs863224928
Exacrs863224928
Varsomers863224928
Maprs863224928
PheGenIrs863224928
hapmaprs863224928
1000 genomesrs863224928
hgdprs863224928
ensemblrs863224928
gopubmedrs863224928
geneviewrs863224928
scholarrs863224928
googlers863224928
pharmgkbrs863224928
gwascentralrs863224928
openSNPrs863224928
23andMers863224928
23andMe allrs863224928
SNP Nexus

SNPshotrs863224928
SNPdbers863224928
MSV3drs863224928
GWAS Ctlgrs863224928
Max Magnitude0
ClinVar
Risk rs863224928(A;A)
Alt rs863224928(A;A)
Reference rs863224928(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.152712499C>T
CLNSRC
CLNACC RCV000200158.1,