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rs606231292

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231292(C;T)
Make rs606231292(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position152354817
GeneSYNE1
is asnp
is mentioned by
dbSNPrs606231292
ebirs606231292
HLIrs606231292
Exacrs606231292
Varsomers606231292
Maprs606231292
PheGenIrs606231292
hapmaprs606231292
1000 genomesrs606231292
hgdprs606231292
ensemblrs606231292
gopubmedrs606231292
geneviewrs606231292
scholarrs606231292
googlers606231292
pharmgkbrs606231292
gwascentralrs606231292
openSNPrs606231292
23andMers606231292
23andMe allrs606231292
SNP Nexus

SNPshotrs606231292
SNPdbers606231292
MSV3drs606231292
GWAS Ctlgrs606231292
Max Magnitude0
ClinVar
Risk rs606231292(T;T)
Alt rs606231292(T;T)
Reference rs606231292(C;C)
Significance Pathogenic
Disease Spinocerebellar ataxia
Variation info
Gene SYNE1
CLNDBN Spinocerebellar ataxia, autosomal recessive 8
Reversed 1
HGVS NC_000006.11:g.152675952G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144953.3,